Note: Descriptions are shown in the official language in which they were submitted.
1~88S35
PHARMACEUTICALLY ACTIVE 2-SUBSTITUTED-l- -~
(OMEGA-AMINOALKOXY)BENZENES
. BACXG~OUND OF THE IN~N~ON
Fleld Or the Inventio~
This invention relates to 2-substituted-1-(omega-aminoalkoxy)
benzenes which are pharmacologically active as antidepre~sants.
DescriPtion o~ the Prior ~rt
L. C. Cheney et al, J. Am. Chem. Soc., Vol. 71, 60-64 (1949)
deocribeo Jeveral diphenylmethanes contalning a sub~tituent
at the 2-position, including 2-dimethylaminoethoxy, 2- -
diethylaminoethoxy, 2-morpholinoethoxy, 2-(1-piperidyl)ethoxy,
2-ioopropylaminoethoxy, 3-(1-piperidyl) propoxy, 3-dimethyl-
aminopropoxy and 3-dibutylaminopropoxy.
That re~erence al~o indica~es that 2-(2-aminoethoxy)diphenyl-
; met~ano~ and 2-(3-aminopropoxy)diphenylmethanes have anti-
hiotaminic and local ae~thetic activity in animals. ~-
- However, it is to be noted that the 2-(4-aminobutoxy)diphenyl-
methanes and 2-(5-aminopentyloxy)diphenylmethane~ of this
invention are not deocribed in that reference
It is al~o to be noted that there i9 no indication in that
reference that the 2-omega-aminoalkoxydiphenylmethanes
poooess antidepressant activity.
A~ a matter Or fact, the 2-(3-dimethylaminopropoxy)diphenyl-
methane which is described in that reference does not pos~ess
,,
~; antidepr-s~ant activity according to ph~rmacological testing.
.
_ 2 -
1~88S35
SUMMARY OF THE INVENTION , - .
.
This invention in one aspect relates to the preparation of
compounds of the formula (I):
O- ~ CH2 ) nRl
~ R2 (I) ~.
and a pharmaceutically acceptable acid addition salt thereof, ~-
wherein Rl is selected from the group consisting of amino, Cl-C5 a-lkylamino,
C2-C6 dialkylamino, morpholino, l-piperidyl, 4-methyl-1-piperazinyl and ~ ,~
l-pyrrolidinyl; R2 is selected from the group consisting of benzyl,.phenoxy,
phenylthio and l-phenylethyl; and n is an integer of 3, 4 or 5; with the ~;
provisos that when R2 is phenoxy and n is 3, Rl is amino or Cl-C5 alkylamino;
when R2is phenoxy and n is 4 or 5, R1 is amino, Cl-C5 alkylamino, C2 - C6
dialkylamino msrpholino, l-piperidyl, 4-methyl-1-piperazinyl and .....l-pyrrolidinyl; when R2 is benzyl and n is 4 or 5, Rl is C1 - C5 ~.
alkylamino or l-piperidyl; and when R2 is benzyl and n is 3, Rl -.
i9 Cl - C5 alkylamino, which comprises reacting a 2-substituted-
i-(omega-halogenoalkoxy) benzene of the formula (II): . .. --
0-(CH2)nX .
wherein X is a halogen; and R2 and n are as defined.above, with.an amine of
the formula (111): -
R1 ~ H (Ill) .:
wherein Rl is defined above, and if desired reacting the
~: compound with a suitable acid to yield the pharmaceutically :.
: aceeptable acid addition salt. .:
~ -
,,~ .
~8535
The compound palLiates conditions of depression in warm-blooded
animals when administere~ to the animal in an antidepressant
effective amount.
, . ,
DESCRIPTION OF ~HE INVENTION ~-
A~ summarized abo~e, this invention relates to a group of
compounds uJerul a~ pharmaceutical agentq, which compound~
are represented by Formula I above.
Illu~trative Or the compounds of thi~ invention are the
following:
10 . 2--(4-aminobutoxy)diphenyimethane
2-(4-methylaminobutoxy)diphenylmethane
2-(4-ethylaminobutoxy)diphenylmethane
2-~4-dimethylaminobutoxy)diphenylmethane
2-(5-methylaminopentyloxy)diphenylmethane
2-t5-dimethylaminopentyloxy)diphenylmethane
2-(4-morpholinobutoxy)diphenylmethane
2- ~4-(1-piperidyl)butoxy~ diphenylmethane
4- ~4-(4-methy}-1-piperazinyl)butoxy ~diphenylmethane .
2-(3-methylaminopropoxy)diphenyl ether
2-(3-dimethylaminopropoxy)diphenyl ether
2-(4-aminobutoxy)diphenyl ether
2-(4-methylaminobutoxy)diphenyl ether
~' ' ' ....
: .
- 4 -
1(~88S35-
2-(4-dimethylaminobutoxy)diphenyl ether
2-(4-morpholinobutoxy)diphenyl ether
2- (4-~4-methyl-1-pipèrazinyl)butoxy ~ diphenyl ether
2-(5-methylaminopentyloxy)diphenyl ether
2-(5-dimethylaminopentyloxy)diphenyl ether
2- ~5-(1-piperidyl)pentyloxy ~diphenyl ether
2-(3-methylaminopropoxy)diphenyl ~ulfide
2-(3-dimethylaminopropoxy)diphenyl sulfide
' 2-(4-aminobutoxy)diphenyl sulride
2-(4-methylaminobutoxy)diphenyi sulfide
2-(4-dimethylaminobutoxy)diphenyl ~ulfide : :
2-(4-morpholinobutoxy)diphenyl sulfide ~ -
2- ~(4-methyl-1-piperaziny~)butoxy ) diphenyl sulfide
2-(5-methylaminopentyloxy)diphenyl ~ulfide
2-(5-dimethylaminopentyloxy)diphenyl ~ulfid~
2- ~4-(1-piperidyl)butoxy ) diphenyl sulfide
2-(3-methylaminopropoxy)diphenylmethane
2-(3-ethylaminopropoxy)diphenylmethane
2-(3-methylaminopropoxy)diphenylmethylmethane
2-(3-dimethylaminopropoxy)diphenylmethylmethane
2-(4-aminobutoxy)diphenylmethylmethane
2-(4-methylaminobutoxy)diphenylmethylmethane
2-(4-dimethylaminobutoxy)diphenylmethylmethane
2 (5-methylaminopentyloxy)diphenylmethylmethane
2-(5-di~methylaminopentyloxy)diphenylmethylmethane
~ . ,
~(~88S35
The pharmaceutically ac¢eptable acid addition salts Or the
above compound~ are, Or cour~e, also included within the
~cope Or this invention.
It will be understood that the term "pharmaceutically
acceptable acid addition salt~" a~ used herein i9 intended !
to include non-toxic salts Or the compound~ Or this inven-
tion with an anion. Repre~entative Or ~uch salts are
hydrochlorides, hydro~romide~, sulrate~, phosphates, nitrates,
a¢etates, ~ucdinates J adipates, propionates~ tartrates,
maleates, citrates, benzoate8, toluenesulfonates, and
m-thanesulronates.
or the compounds of this invention, it will be understood that
the following compounds are most preferred due to their high
level Or antidepressant activity and their low level of
toxicity.
,
:,
,"
`~ "~ ' .
. 1088S35 ::
2-(4-methylaminobutoxy)diphenylmethane
2-(4-ethylaminobutoxy)diphenylmethane
2-(5-methylaminopentyloxy)diphenylmethane
2-(4-methylaminobutoxy)diphenyl ether :
2-(~-dimethylaminobutoxy)diphenyl ether ...
2-(5-methylaminopentyloxy)diphenyl ether
2-(3-methylaminopropoxy)diphenyl sulride ;~ :
2-(4-methylaminobutoxy)diphenyl qulfide -
2-(4-dimethylaminobutoxy)diphenyl sul~ide
2-(5-methylamdnopentyloxy)diphenyl ~ul~ide :
2-(3-methylamlnopropoxy)diphenylmethane
2-(4-methylamlnobutoxy)diphenylmethylmethane . .
2-(4-dimethylaminobutoxy).diphenylmethylmethane
2-(3-dimethylamlnopropoxy)diphenylmethylmethane
pREPARATION
The compounds of thi~ in~ention are prepared by reacting a
2-~ubstituted-1-(omega-halogenoalkoxy)benzene with an amine.
The 2-substituted-1-(omega-halogenoalkoxy)benzene starting
materiala which are represented by Formula II above can be
prepared by reacting a 2-substituted phenol with a 1,3-.
. . dihalogenopropa~e, 1,4-dihalogenobutane or 1,5-dihalogeno-
pentane in the presence o~ an alkali.
~'~'' ' ' , .
., , .i~
1~88535
The amine starting material~ which are represented by
Formula m abo~e lnclude ammonia; primary amine~ such as
methylamine, ethylamine, lsopropylamine and the like;
secondary amines such a~ dimethylamine, diethylamine~ N-
methylethylamine and the like; morpholine; piperidine;
4-methylpiperazine; and pyrrolidine.
The amine reacts with the equimclecular amount of the 2-
~ubstituted-l-(omega-halogenoalkoxy)benzene. However, the
use of the exce~s am~ne accelerates the reaction. Normally,
10 . the amount of the amine to be employed i9 in the range of
1 to 100 moles per mole of the 2-substituted-1-(omega-
halogenoalkoxy)benzene. . ~-.
The reaction can be carri6~d out without an added solvent.
However, the use of a reaction-inert solvent makes a homo-
genous reaction poSsible.
Examples o~ such solvents are water, dioxane, tetrahydrofuran,
dimethyl 9ulfoxide, lower aliphatic alcohols and the mixture
thereof.
The reactlon temperature i8 not critical, but normally
ranges from room temperatures to 150C.
The reaction time varie~ widely with the reaction temperature
and the reactivity Or the starting materials, but normally
is in the range of from 10 minutes to 40 hours.
The pre~ence of bases wkich neutralize a hydrogen halide
formed in the course of the reaction accelerates the reaction. ~`
1088S35
Examples of ~uch bases are inorganic bases such as po- .
tassium hydroxide, sodium hydroxide, potassium carbonate, - -
Oodium carbonate and the like; and tertiary anine~ such as
pyridine, triethylamine and the like. ~-
The amount Or the base to be employed is normally in the
range Or I to 5 moles per mole of the 2-substituted-1-
(omega-halogenoalkoxy)benzene.
When the baae i~ aboent, the 2-subst~tuted-1-(omega-
aminoslkoxy)benzenes react with a hydrogen halide formed
during the reaction, and are con~erted to the acid addi- ' -~
tion aalt9 thereof.
Ac~d addition salts Or the 2-substituted-1-(omega-aminoalkoxy)
benzeneJ may be ¢onveniently prepared by contacting the
oompound~ with a ~uitable acid.
The 2-~ubstituted-1-(omega-aminoalkQxy)benzene# and the acid
addition ~alts thereof may be purified by recry~tallization
:: employing a ~uitable solvent ~uch a~ al¢ohol-ether.
Pharmacological testing Or the 2-sub~tituted-1-(omega-
aminoalkoxy)benzenes has demonstrated that they are u~eful - -
as antidepressant agents as evidenced by their ability to
rever9e re9erpine hypothermla in mice.
:~ The compound9 have been te~ted in mice for antidepressant, -:
.,
- ~ .
~ . . .-- .
1~88S35
~edative, anticonvulsant and anticholinergic activity.
T~e compounds were administered intraperitoneally and the
activities of the compound~ were compared with those of
Amitriptyline.
Antidepres~ant activity was evaluated by antagonism of
reserpine (5 mg/kg i.p.) induced hypothe~mia (P.S.J. Spencer
in "Antidepressant DrugY" S. Garattini and M.N.G. Duhes,
ed., Excerpta Medica Foundation, Amsterdam, pages 194-204
(1967)) and antireserpine activity was expressed as rela-
tive potency (Amitriptyline = 1).
LD50 was calculated by Lltchfield-Wilcoxon method.
CNS depressant activity was defined by the ability of the
compounds to cause neurol~gical deficit as measured by
traction test (S. Courvoisier, R. Ducrot, L. Julou;
"P~ychotropic Drugs" ed. by S. Garattini, V. Ghetti, page
373, (1957)) and spontaneous motor activity (Spontaneous
motoi activity was measured by ANIMEX apparatus).
Anticon w lsant activity was determined by antagonism of
electroshock induced tonic extensor (L. S. Goodman, M.
Singh Grewal, W. C. Brown and E. A. Swinyard, J. P~armacol,
Exptal. Therap., 108, 168 (1953)).
Central anticholinergic effect was asse~sed by testing the
tre rine induced tre r in mice (G. M. E~erett, L. E.
Bloucus and J. M. Sheppard, Science 124 79 (1956)).
.', .~
.
-- 10 --
1088S3S
.. -.
Result~ are summarized in Table 1 and Table II, in which
EDS i9 de~ined a~ the dose Or the test compounds, which
pre~ent 50% of each re~ponse. :;
Table I. Antire~erpine Activity in Mice .
~ .
. _ . ..
Compound Relative LD50 ~
Potency (mg/kg i.p.) ..
.. _ . , . _ . . ... ,., _. ~ ~ ._
2-(4-methylaminobutoxy)diphenyl- 0 73 .
methane hydrochloride . 73
. . , .
2-(4-ethylaminobutoxy)diphenyl-0 3 2
methane hydrochloride .5 1 0
.. _ . .
2-(5-methylaminopentyloxy)diphenyl- .
Dethane hydrochloride O.5 160 ~.,
_ . . .
2-(3-dimethylaminopropoxy)- . .
diphenylmethane hydroch}oride 0.00
.~___ . . _ , . ',,
2-(4-methylaninobutoxy)diphenyl
ether hydrochloride 1.10 100
. I `:
2-(4-dimethylaminobutoxy)- .
diphenyl ether hydrochloride 0.S8 . 92
2-(5-methylaminopentyloxy)- 0 :
diphenyl ether hydrochloride 57 85
__ . . . .,
2-~4-methylaminobutoxy)diphenyl 0 0 .
~ulfide hydrochloride .9 120
.. . _
2-(4-di~ethylaminobutoxy)- -~
diphenyl ~ulfide hydrochloride . 0.70 130
2-(3-methylaminopropoxy)- 0 6
diphenyl ~ulfide hydrochloride . 0 13S
... _. .
::~ 2-(3-methylaninopropoxy)diphenyl-
methane hydrochloride 0.56 160
. :'
,
, .
:
1~88S35
. .
Compound Relati~e LD50
. ~ . . Potency (mg/kg i.p.)
~ .
2-(3-dimethylaminopropoxy)diphenyl- 0 00 .
methane hydrochloride . _
._
2-(2-dimethylaminoethoxy)diphenyl-0 00
. methane hydrochloride . _
. . ::
2-(2-methylaminoethoxy)diphenyl-
methane hydrochloride 0.00 _
. __
2-(4-methylaminobutoxyjdiphenyl- ~ .
methylmethane hydrochloride . o.66 140
- - . . . __ _
2-(4-dimethylaminobutoxy)diphenyl-
methylmethane hydrochloride 0.36 110 :~ :
. _ _ .
2-(3-dimethylaminopropoxy)-
diphenylmethylmethane hydrochloride 0.34 155
. . . .
~ 1.00 65
.. ~. .:
~ ~ .
,,.. ,~ ~ .
~: .
~ ,
- 12 _
.
1~88S35
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-- 13 --
1~8853S
It will be apparent from Table~ I and II that the 2-~ubsti-
tuted-l-(omega-aminoalkoxy)benzenes exhibit antireserpine
activity comparable to that of Amitriptyltne~ while they
exhibit low toxicity, weak CNS depressant and anticholinergic
action.
The compounds Or thi~ invention can be admini~tered by any
mean~ that effects palliatin~ conditions Or depre~sion in
warm-blooded animal~.
For exsmple, administration can be parenterally, sub-
cutaneously, intra~enously, intramuscularly~ or
~ntraperitoneally. Alternati~ely or concurrently, adminis-
tration can be by the oral route. The dosage administered
will be dependent upon th~ age, health and weight of the
recipientJ the extent Or depression, kind of concurrent
treatment ir any, frequency of treatment, and the nature
Or th- effe¢t de~ired. Generally, a daily dosage of the
active ingredient compound will be from about 0.5 to 50 mg
.~, , .
per kg of body weight. Normally, from 1 to 30 mg per kg
per day, in one or more applications per day i~ effecti~é
to obtain the desired re~ult.
The compound of Formula I can be employed in dosage form~
~uch a~ tablets, cap~ule~, powder packets, or liquid solu-
.,:.
tions, YuspenSion~ or elixirs, for oral administration, or
sterile liquid formulations such a~ ~olution-~ or suspensions
~`
'~,' ^ .
.-
.
.... .
:,:
: _ 14 --
-. .
,
-- .
. .
1~88S35
for parenteral use. In such compositions, the actire in-
gredient will ordinarily always be present in an amount of
at least 0.5% by weight based on the total weight Or the
composition and not re than 90~ by wei~ht.
Beside~ the active ingredient Or this invention, the com-
~ .
position will contain a sol1d or liguid non-toxic phar-
maceutical carrier for the actire ingredient. In one
embodimont Or a composition, the solid carrier can be a
capsule of the ordinary gelatin type. In the capsule will
be from about 30-60% by weight Or a compound Or Formula I
and 70-40% Or a carrier. In another embodiment, the act~ve
ingredient can be tableted with or without ad~uvants, or
put into powder packets. ~These capsule~, tablets and ~;
powders will generally constitute from about 5% to about 95%
and preferably from 2S% to 90% by weight Or the a¢tiYe in-
gredient. The~e dosage ~orms preferably contain rrom about
5 to about 500 me of actire ingredients, with from about
25 to about 250 mg being st preferred.
The pharmaceutical carrier can bQ a sterile liquid suc~ as
~0 water and oils, including those Or petroleum, animal, Yege-
table or synthetic origin, such as peanut oil, soybean oil,
mineral oil, sesame oil, and the like.
In general, water saline~ aqueous dextrose and related sugar
solutions, and glycols such a~ ethylene glycol, propylene
glycol and polyethylene glycol are preferred liquid carriers,
.
:
~ - 15 -
1~88S3S
particularly for injectible solutions ~uch as saline will
ordinarily contain from about 0.5% to 20% and preferably
about 1 to 10% by weight of the active inBredient.
As mentioned above, oral admini3tration can be in a suita- ;
ble suspension or syrup, in which the active ingredient
normally will constitute from about 0.5 to 10% by weight.
The pharmaceutical carrier in such compo~ition can be a
watery vehicle such a~ an aromatic water, a syrup or a
pharmaceutical mucilage.
The following exa~ple9 are presented to rurther illu~trate , : ;
the preparation of the compounds of thi~ invention. : -
Example 1 ~ -~
~ .
A Aolution o~ 5.0 g Or 2-(4-bromobutoxy)diphenyl ether~30 ml
of 40% dimethylamine aqueous solution, and 100 ml Or ethanol
~8 allowed to ~tand at room temperature for 8 hours. Ethanol
ahd éxcea9 dimethylamine are distilled in vacuo, 2N-NaOH
aqueous solution i8 added, and the reaction product is
extracted with ether. The ether solution is distilled, 2N-
HCl solution i8 added and the solution is evaporated to
dryness. .
The re~idue is recrystallized from ethanol-ether to give
4.6 g (89~ yield) of 2-(4-dimethylaminobutoxy)diphenyl ether
hydrochloride, m.p. 131-135C.
, -.
_ 16 _
1~88535 : ~
.
Analysi~ - Calcd. for C18H23N02-HCl (percent): C, 67.17;
H, 7.S2; N, 4.35
Found (percent): C, 67.35; H, 7.46; N, 4.25
. . ~
Example 2
A oolution Or 5.0 g of 2-(5-bromopentyloxy)diphenyl ether
and 6 g of methylamine in 100 ml o~ ethanol i8 heated at
a temperature Or 50& for 2 houro in a ~ealed tube.
Fthanol and exceJs methylamine are distilled in vacuo, 2N-
NaOH agueous solution i~ added, and the reaction product
0 i8 extra¢ted with ether. Dry hydrogén chloride gao lo
paosed into the ether ~olution, and the precipitate col-
l-oted by flltration. Recry~tallization from ethanol-
ether gi~eo 4.2 g (88% yield) Or 2-(5-methylaminopentyloxy)-
diphenyl ether hydrochloride, m.p. 88 - 90C.
Analyoio - Calcd. for C18H23N02-HCl (percent): C~ 67.17;
H, 7.~2; N, 4.35
Found (percent): C, 67.30; H, 7.64; N, 4.37
,,` ~ :
~ - 17 -
1~88S35 `
`'
Examples 3-38 ~ :~
The compounds in the following table were prepared according
to the procedure described in Example 1 or 2 using the
appropriate starting materials. ~ ~:
- 18 -
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1~88S35
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88535
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1~8S35
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Having now fully de~cribed the invention, it will be apparent
to one Or ordinary skill in the art that many changes and
modirications can be made thereto without departing rrOm
the spirit or scope Or the invention a~ ~et forth herein.
,
- 28 ~