Note: Descriptions are shown in the official language in which they were submitted.
3~
NOVEL DERlVATlVES OF EBURNAMONINE ANV RELATED ME-
THOD OF MAI`IUFA.CTU RING "
O O O O O O
The present invention relates to novel derivatives of eburnamonine
having interesting therapeutical properties at the cerebrovascular
level, and more particularly having cerebral vasodilating action, u
seful for the prevention and the treatment of the cerebro-vascular
diseases .
The eburnamomine (the laevorotatory form of which is known as vin
camone) having the formula (I):
~ ' (I)
is a compound already known and used in the therapy of the cerebro-
vascular diseases, due to the efficacious vasoregulating action thereof
at the cerebral level and also due to its capability of activating the
metabolism of the nervous cells.
The eburnamonine in the dextro-~aevo-rotatory and racemic forms
has been the subject of rather intense studies as regards the structu-
re and characterization, as well the preparation thereof. In this con-
nection there are known and reported in the literat~re:
1. processes for its extraction and isolation from several vegetable spe
cies, belonging to the family of Apocinaceae (for instance, Hunteria e-
burnea, Amsonia tabernaemontana, Vinca m~ etc.)~~DT-OS
1,933,110; DT-PS 1,187,031; Doepke et al., Pharmazia, 21 (7),
~i/l/l (1966) etc.)
2) partial synthesis processes, starting from natural alkaloids, su-
ch as for example those described in the Hungarian patent No. 151,2957
in the French patent No. 2,209,757, in the paper by Hugel G. et al.,
Bull. Soc. Chim. Franc. 1965, 2497, etc.
3) total synthesis processes; such as for example -those described
in:
- Bartlett M.E. et al., Tetrahedron Lett., 1959, 20;
- Werkert E. e-t al., J. Am. Chem. Soc., 87, 1580, 1965;
- Belgian patents Nos . 776 ,337 and 802 ,913 .
However the therapeutical effec-t thereof, through the several admi-
nistration routes, is characterized by a short duration, as caused by
the quick elimination thereof, whereby several administrations are
needed in the 24 hour period.
It has been now found, and it is the object of the present invention,
that some salts of the vincamone are e~dowed with a like therapeutical
activity together with a time delayed effect, namely- have the so-cal-
led long-acting effect, these salts having the following general formu-
la (II):
~ N X
0//~ - 2 -
Et
~ 7 ~
wherein X represents the radical of a compound selected in the class
comprising glucose-l-phosphate acid, clo~ibric acid, acetylsalicy-
lic acid, pamoic acid, 2,4-dihydroxyben~oic acid, 3,5-dihydroxy-
benzoic acid and pivalic acid. Among the above compounds, -the e-
quimolar association of vincamone and glucose-l-phosphate sodium
salt is furthermore of interest.
The general process for the preparation of the compounds of the in-
stOc~, 0,~ ,ca/
vention comprises reacting, in stechio~nctrical ratio, the-vincamone,
which according to the desired derivative is in form of a solution or
suspension in lower aliphatic alcohol, chloroform or their mixtures,
with the acid, preferably in form of a solution in a lower aliphatic al
,o~c~ v~
cohol or water, the reaction being effected,~rhot ~at a tempe-
- rature controlled by the boiling point of the solvent mixture and under
stirring, until the reaction is completed, the reaction product being
thereafter separated by filtration or by concentration to a residue of
the reaction mixture.
The following examples detailedly illustrate the presen-t invention.
EXAMPLE 1
Vincamone glucose-l-phosphate bisodium salt
This compound is in fact an equimolar association, the raw formula
being ClgH22N20. C6HllNa209P, whereas -the structural formula is
as follows:
~ P_Olla
0~
~-2 ~inca~o~ e
_~ 5.9 g (2.10 moles) of ~-~Pws~ are disso]ved in a mi~ture of
'~ ethanol and chloroform, the solution being prepared uncler heaciny
in a water bath and under stirring.
Then a solution of 6.9 g of glucose-l-phosphate bisod-
ium salt tetrahydrate in the minimurn amount of water is added
dropwise and the mixture is maintained at 70C ancl under stirrin~
for 30 minutes and then concentrated at the-- ~ pres-
sure to a small volume. Then 80-lO0 mls OL ethanol are added
and the solvent is distilled to a residue. This ste~ is repeated
two times, the reaction mixture being finally brouht to a vol- -'
ume of a~out l5 to 20 mls.
The precipitation of the reaction product is completed ;`
by maintaining the reac-tion mixture on standing in an ice bath.
After filtration and drying of the product in an air
circulation oven at 60C, about ll g are obtained of a white
crystalline substance, which is not soluble in water and alcohol,
having total melting point of about l80C.
T~e content of vincarnone in this adduct is 49QO.
E~IPI.E 2
~eutral vincamone ~lucose-l~phosphate
--
O H OH OH
,
iL$~
5.9 g (2.10 mol- s) of vincamone are suspended in a mixture of 250
mls of ethanol and 40 mls of chloroforrrl.
The suspension is heated to 70C i a water bath, under stirring,and
is dropwise added with a water solution of 2.6 g (10 moles) of gluco-
se-1-phosphate acid.
The mixture is main-tained under stirring and at the boiling point for 30
minutes and then concentrated to a small volurne under reduced pressu-
re .
The r~sidue is taken with 2 x 200 mls ethanol and finally concentrated
to 80 mls.
The product is crystallized by putting the reactor in an ice bath.Af-
ter filtration and drying in an air circulating oven at 70C, there a-
re obtained about 7 g of a white, crystalline, solid product, which is
insoluble in water and alcohol.
m.p.: about 170C (with decomposition).
The vincamone dosage in the salt is 66%.
EXAMPLE 3
Vincamone glucose - 1-phosphate, acid salt
~ /\ CH20H
\N~/ H~O--1~
\ H 01-1
~ \/
Et
~7~ ~
25 35N210P - M W- = 554.5
The example 2 is repeated, except that 5.9 g (2.10 moles) o~-vi-n
camone and 5.2 g of glucose-1-phosphate acid are used.
There are obtained about 10 g of a white, crystalline product, so-
luble in water and having melting point of abou-t 175C with decom-
position .
The vincamone content of the salt is 50%.
EXAMPLE 4
Vincamone 2,4-dihydroxy-benzoate
~) \\
lS Et
C26H28N205 - M.W.= 448.5
A suspension comprising 5.9 g ( 2.10 moles) of vincamone and
100 mls of ethanol is heated to boiling and then gradually added
with a solution of 3.1 g (2.10 moles) of 2,4-dihydroxybenzoic
acid in ethanol.
The boiling condition is maintained for about one hour, possibly
adding chloroform so as to obtain a homogeneous solution. The
reaction mixture is then concentrated under reduced pressure to
a small volume and the precipitation of the salt is completed by
- 6 -
.
, . , . ~
.. .
diluting with ethyl ether. Af-ter filtra-tion and drying in an air circu-
lating oven at 60C, there are obtained about 8 g of a salt, water
insoluble and poorly so~uble in alcohol, having melting point of 183-
-185C .
The vincamone content of the salt is 65.5%.
EXAM P LE 5
Vincamone 3,5-dihydrox~ben7Oate
COOH
0 ~N HOJ~\OH
26 28 2 5 44 5
The preparation is carried out according to the precise conditions
of the preceding example.
There are obtained about 8.5 g of a white, crystalline product,inso-
luble in water and poorly soluble in alcohol, having melting point of
185-187C. In this case the vincamone content of the salt is slightly
lower than that found in the preceding example
EXAMPLE 6
Vincamone acetylsalicylate
C 8H30N205- M.W.= 474.6
A solution of 3.6. g (2.10 moles) of acetylsalicyclic acid in 30 mls
of ethanol is added -to a solution of 5.9 g (2.10 moles) of vincamone
,:
.
~7~
in a mixture of ethanol and chloroform.
The mixture is maintained to boiling under stirring for 10 minutes,
concentrated to a small volume, taken with ethanol and then the sol-
10 vent is evaporated until a final volume of 10 mls is attained. The saltprecipitation is completed by adding ether, the mixture being cooled
in an ice bath.
After filtration and drying in an oven under vacuum at 40C,
about 8 g of a product insoluble in water, poorly soluble in al-
cohol and having total melting point of about 150C.
The vincamone content is about 59.1%
EXAMPLE 7
Vincamone pivalate
~ CH3--C--COOH
25C24H32N203- M.W.= 396.75
11 g of this salt are prepared, according to the conditions of the
, , . ,, : ~. ~ , i. ..
preceding examples, starting from 8.83 g (3.10 moles) of vincamo-
ne and 3.06 g (3.10 2moles) of piva~c acid. The resulting product
is insoluble in water, poorly soluble in alcohol and does totally melt
at 168C.
The vincamone content of the salt is 74.6%.
EXAMPLE 8 Cl
Vincamone clofibra~e ~ ~3
CH3--C-COOH
C29H33Cl N204 - M.W.= 509 CH3
The procedure of the examples 5,6 and 7 is repeated starting from
5.9 g ( 2 .10 2moles) of vincamone and 4.3 g (2 .10 moles) of clofi~
bric acid.
15 The final product (about 9 g) is a low melting solid (at 65C), with
a total melting occurring at 135C, which is insoluble in water and
poorly soluble ir: alcohol, the vincamone content being 50 . 3%
EXAM P LE 9
r O~ ~ CH2
L ~ 2 ~ COOH
? ~
59 60 4 8 977
S.9 g (2.10 moles) o:F vincamone are dissolved in 20 mls of N HCl;
possibly adding a small amount of methanol to prom ,te the solving
of the substance.
A solution comprising 3.88 g (10 moles) of pamoic acid in 20 mls
of N NaOH is separatedly prepared and dropwise added under stir-
ring to the vincamone solution.
Upon the addition is completed, the stirring is continuated for 10
minutes further, the precipitate is filtered, washed with water in-
to the filter and then dried in an oven under reduced pressure at
80C .
There are obtained about 8 g of a product, insoluble in water and
alcohol, ha~-ring total melting point of 175C.
The vincamone content of the salt is 60.9%.
The novel derivatives according to the invention have been tested
from the pharmacological point of view, and the following prope:r-
ties have been particularly examined:
- acute toxicity by intraperitoneal route;
- hematic levels and urinary recovery;
- variations of the hematic flow in the cerebral ar-teria as well as
of the cerebro-vascular resistances.
A-acute toxicity
The acute toxicity has been determined in the mouse, type COBS
CD-1 (Charles River), having an average body weight of 20-25 g
and of male sex., groups of three animals being used and evaluated
on the basis of the average lethal dose (observation time: 8 days)
- 10 -
The compounds were administered as a suspension in 1% car~oxyme-
thylcellulose .
-The results of the tests of acute toxicity confirmed that the compounds
of the invention, when administered by the parenteral route are scar-
cel y toxic .
B- Absorption
All the compounds have been orally administered a-t the dosage of
1OO mg/kg, expressed as vincamone, in form of a suspension in
1% carboxymethylcellulose, to albine male rats, G~` the COBS type
and of average body weight of 250 g.
The absorption was determined by evaluating the hematic levels
at the following times (minutes):O, 30,60, 120,240,360, and 480.
There was also assessed the urinary elimination at the following
times (hours): 8, 24 and 48.
The vincamone concentrations were determined by the chromato-
graphic me-thod.
All the tested compounds show a good absorption followed by a
quick elimination. More particularly, from the abs~orptio~ data,
as reported in Table 1, it can be appreciated that the compound
of example 3 shows a relevant " deiayecl", effect. A greater bio-
-availability with respect to the vincamone is also shown by the
compounds of the examples 5, 7 and 9.
C- Hematic flow
The cerebral vasodilating activity was studied in Beagle dogs,
f average body weight of 15 kg, the animals being anestetized
with sodium Thiopental (30 mg/kg i p.) . The right vertebral ar-
, - ., ~ . ~ , .
,; ..~ .
tery of the animals was isolated and the hematic flow was recorded
by means of a flow transducer connect~d to an electromagnetic flow-
meter Statham SP 2201, in turn connec-tcd -to a Med.ium Gain Ampli-
fier Hewlett Packard 8802A.
TABLE 1
Hematic levels (as/ug/ml) of vincamone after administration per os
in the rat of the deri~ati.ves of the invention
Compound Time from the administration, hours
0.5 1 2 4 6 8
Example 1 1,07 1.69 0.94 0,65 0.18 ----
Example 2 1~62 2.63 1.06 traces ---- ------
Example 3 traces 0.13 0.79 0.82 1.69 1.28
Example 4 0.15 1.34 1.30 traces ----- ----~--
Example 5 0.13 1.78 2.37 1.39 0.68 traces
Example 6 N.D. N.D. N.D. N.D.N.D. N.D.
Example 7 0.18 3.01 2.95 1~05traces ------
Example 8 N.D. N.D. N.D. N.D. N.D. N.D.
Example 9 1.191.27 1.55 1.32 traces ----
Vincamone 1.372.20 1 .04 0.42 traces -----
N.D. not determined
The arterial pressure in the right femoral artery was also recorded
by means of a Hewlett Packard l280C transducer, in turn connected
to a Carrier Amplifier Hawlett Packard 8805B.
- 12
. .
The compounds ~vere administered by intravenous route in the right
femoral vein at doses corresponding to 4 mg/kg of vincamone.
For the evalu-tazion ~f the vasodilating effect of the vincamone deri-
vatives, both the percent variations of the cerebral flow as caused
by the compounds of the invention and the maximum percen-t variation
of the cerebrovascular resistance were compared.
The results confirmed that all the tested compounds have vasodilating
action at the level of the right vertebral artery which controls the
cerebral circulation.
o O o o o
- 13 -
', ;