Method for preparing pyrrolidine oximes
The present invention is related to a new synthesis for preparing pyrrolidine oximes of general formula (I). The compounds of formula (I) are useful in the treatment and/or prevention of preterm labor, premature birth and dysmenorrhea.
1 . A method of preparing a compound according to formula (I):
wherein
A is a carbonyl group —(C═O)—;
B is selected from the group consisting of an oxadiazole ring, an amido group of the formulae —(C═O)—NR 3 R 4 , and —(CH 2 )n—X—R 8 ;
wherein the oxadiazole ring is any of the formulae:
R 1 is H or a C 1 -C 6 -alkyl;
R 2 is selected from the group consisting of aryl, heteroaryl and saturated or unsaturated 3-8-membered cycloalkyl;
R 3 and R 4 are independently selected from the group consisting of hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, alkoxy, sulfanyl, acyl, alkoxycarbonyl, aminocarbonyl, saturated or unsaturated 3-8-membered cycloalkyl which may contain 1 to 3 heteroatoms selected of N, O, S, aryl, heteroaryl, C 1 -C 6 -alkyl aryl and C 1 -C 6 -alkyl heteroaryl;
X is O or NR 9 ;
R 8 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkyl aryl, heteroaryl, C 1 -C 6 -alkyl heteroaryl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkenyl aryl, C 2 -C 6 -alkenyl heteroaryl, C 2 -C 6 -alkynyl, C 2 -C 6 -alkynyl aryl, C 2 -C 6 -alkynyl heteroaryl, C 3 -C 8 -cycloalkyl, heterocycloalkyl, C 1 -C 6 -alkyl cycloalkyl, C 1 -C 6 -alkyl heterocycloalkyl, C 1 -C 6 -alkyl carboxy, alkyl, C 1 -C 6 -alkyl acyl, C 1 -C 6 -alkyl acyloxy, C 1 -C 6 -alkyl alkoxy, alkoxycarbonyl, C 1 -C 6 -alkyl alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkyl aminocarbonyl, C 1 -C 6 -alkyl acylamino, C 1 -C 6 -alkyl ureido, amino, C 1 -C 6 -alkyl amino, sulfonyloxy, C 1 -C 6 -alkyl sulfonyloxy, sulfonyl, C 1 -C 6 -alkyl sulfonyl, sulfinyl, C 1 -C 6 -alkyl sulfinyl, C 1 -C 6 -alkyl sulfanyl and C 1 -C 6 -alkyl sulfonylamino;
R 7 is selected from the group consisting of hydrogen, sulfonyl, amino, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, wherein said alkyl, alkenyl, alkynyl chains are optionally interrupted by a heteroatom selected from N, O or S, aryl, heteroaryl, saturated or unsaturated 3-8-membered cycloalkyl, heterocycloalkyl, wherein said cycloalkyl, heterocycloalkyl, aryl or heteroaryl groups are optionally fused with 1-2 further cycloalkyl, heterocycloalkyl, aryl or heteroaryl group, an acyl moiety, C 1 -C 6 -alkyl aryl, C 1 -C 6 -alkyl heteroaryl, C 1 -C 6 -alkenyl aryl, C 1 -C 6 -alkenyl heteroaryl, C 1 -C 6 -alkynyl aryl, C 1 -C 6 -alkynyl heteroaryl, C 1 -C 6 -alkyl cycloalkyl, C 1 -C 6 -alkyl heterocycloalkyl, C 1 -C 6 -alkenyl cycloalkyl, C 1 -C 6 -alkenyl heterocycloalkyl, C 1 -C 6 -alkynyl cycloalkyl, C 1 -C 6 -alkynyl heterocycloalkyl, alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkyl carboxy, C 1 -C 6 -alkyl acyl, C 1 -C 6 -alkyl acyloxy, C 1 -C 6 -alkyl alkoxy, C 1 -C 6 -alkyl alkoxy-carbonyl, C 1 -C 6 -alkyl aminocarbonyl, C 1 -C 6 -alkyl acylamino, C 1 -C 6 -alkyl ureido, C 1 -C 6 -alkyl amino, C 1 -C 6 -alkyl ammonium, C 1 -C 6 -alkyl sulfonyloxy, C 1 -C 6 -alkyl sulfonyl, C 1 -C 6 -alkyl sulfinyl, C 1 -C 6 -alkyl sulfanyl, C 1 -C 6 -alkyl sulfonylamino, C 1 -C 6 -alkyl aminosulfonyl, hydroxy, halogen and cyano;
R 9 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkyl aryl, C 1 -C 6 -alkyl heteroaryl, aryl and heteroaryl;
R 8 and R 9 can form together with the N atom to which they are linked to, a 5-8 membered saturated or unsaturated heterocycloalkyl ring; and
n is an integer from 1 to 3;
said method comprises the following steps:
Step 1: transformation of the pyrrolidine of formula (II) into an acyl derivative of formula (IV) using an acylating agent (III):
Step 2: oxidation of the acyl derivative (IV), with a oxidizing agent, obtaining a pyrrolidone of formula (V):
Step 3: transformation of the pyrrolidone of formula (V) into compound (VII) using a suitable alkoxylamine, aryloxylamine or hydroxylamine of general formula (VI):
Step 4: transformation of the compound (VII) with an amine of general formula (VIII) or an N-hydroxyamidine of general formula (IX) thus yielding compounds (Ia) and (Ib), or transforming compound (VII) first into a nitrile (VIIa), which is then transformed into the hydroxyamidine (VIIb) that is then reacted with a carboxylic acid R 7 —COOH to yield compound (Ic), or first esterifying and than reducing compound (VII) using a suitable esterification or reducing agent, respectively, thus yielding compound (Id):
2 . The method of preparing a compound according to formula (I) according to claim 1:
wherein
A is a carbonyl group —(C═O)—;
B is either an amido group of formula —(C═O)—NR 3 R 4 or an oxadiazole ring of any of the formulae:
R 7 is selected from the group consisting of hydrogen, sulfonyl, amino, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, wherein said alkyl, alkenyl, alkynyl chains are optionally interrupted by a heteroatom selected from N, O or S, aryl, heteroaryl, saturated or unsaturated 3-8-membered cycloalkyl, heterocycloalkyl, wherein said cycloalkyl, heterocycloalkyl, aryl or heteroaryl groups are optionally fused with 1-2 further cycloalkyl, heterocycloalkyl, aryl or heteroaryl group, an acyl moiety, C 1 -C 6 -alkyl aryl, C 1 -C 6 -alkyl heteroaryl, C 1 -C 6 -alkenyl aryl, C 1 -C 6 -alkenyl heteroaryl, C 1 -C 6 -alkynyl aryl, C 1 -C 6 -alkynyl heteroaryl, C 1 -C 6 -alkyl cycloalkyl, C 1 -C 6 -alkyl heterocycloalkyl, C 1 -C 6 -alkenyl cycloalkyl, C 1 -C 6 -alkenyl heterocycloalkyl, C 1 -C 6 -alkynyl cycloalkyl, C 1 -C 6 -alkynyl heterocycloalkyl, alkoxycarbonyl, aminocarbonyl, C 1 -C 6 -alkyl carboxy, C 1 -C 6 -alkyl acyl, C 1 -C 6 -alkyl acyloxy, C 1 -C 6 -alkyl alkoxy, C 1 -C 6 -alkyl alkoxy-carbonyl, C 1 -C 6 -alkyl aminocarbonyl, C 1 -C 6 -alkyl acylamino, C 1 -C 6 -alkyl ureido, C 1 -C 6 -alkyl amino, C 1 -C 6 -alkyl ammonium, C 1 -C 6 -alkyl sulfonyloxy, C 1 -C 6 -alkyl sulfonyl, C 1 -C 6 -alkyl sulfinyl, C 1 -C 6 -alkyl sulfanyl, C 1 -C 6 -alkyl sulfonylamino, C 1 -C 6 -alkyl aminosulfonyl, hydroxy, halogen and cyano;
R 1 is H or a C 1 -C 6 -alkyl;
R 2 is selected from the group consisting of aryl, heteroaryl and saturated or unsaturated 3-8-membered cycloalkyl;
R 3 and R 4 are independently selected from the group consisting of hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, alkoxy, sulfanyl, acyl, alkoxycarbonyl, aminocarbonyl, saturated or unsaturated 3-8-membered cycloalkyl which may contain 1 to 3 heteroatoms selected of N, O, S, aryl, heteroaryl, C 1 -C 6 -alkyl aryl and C 1 -C 6 -alkyl heteroaryl;
said method comprises the following steps:
Step 1: transformation of the pyrrolidine of formula (II) into an acyl derivative of formula (IV) using an acylating agent (III):
Step 2: oxidation of the acyl derivative (IV), with a oxidizing agent, obtaining a pyrrolidone of formula (V):
Step 3: transformation of the pyrrolidone of formula (V) into compound (VII) using a suitable alkoxylamine, aryloxylamine or hydroxylamine of general formula (VI):
Step 4: transformation of the compound (VII) with an amine of general formula (VIII) or an N-hydroxyamidine of general formula (IX) thus yielding compounds (Ia) and (Ib), or transforming compound (VII) first into a nitrile (VIIa), which is then transformed into the hydroxyamidine (VIIb) that is then reacted with a carboxylic acid R 7 —COOH to yield compound (Ic):
3 . The method according to claim 1 , wherein the acyl chloride of step 1 is 1′1-biphenyl-4-carbonyl chloride or 2′-methyl-1′1-biphenyl-4-carbonyl chloride.
4 . The method according to any of claim 1 , wherein the oxidizing agent of Step 2 is pyridine-sulfurtrioxide complex (Py-SO 3 ) in combination with DMSO.
5 . The method according to claim 2 , wherein the reaction is performed in presence of triethylamine.
6 . The method according to claim 1 , wherein the alkoxylamine used in step 3 is O-methylhydroxylamine hydrochloride.
7 . The method according to claim 1 , wherein R 1 is a methyl group, R 2 is a biphenyl.
8 . The method according to claim 1 , wherein B is an amido group of the formula —(C═O)NHR 5 , with R 5 being an C 1 -C 6 -alkyl aryl group.
9 . The method according to claim 8 , wherein R 5 is a phenylethyl group, which is substituted with an amino or hydroxy group.
10 . The method according to claim 1 , wherein B is a 1,2,4 oxadiazole substitutent
with R 7 being a C 1 -C 6 -alkyl or a cycloalkyl optionally containing one or 2 hetereroatoms.
11 . The method according to claim 1 , wherein B is —(CH 2 )n-X—R 8 , with X being O, R 8 being hydrogen; and n being 1.
12 . The method according to claim 11 , wherein the compound is selected from the group consisting of:
(2S,4E and 4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methoxyimino)-1-[(2′-methyl[1,1′-biphenyl]-4-yl)carbonyl]-2-pyrrolidine carboxamide,
(3E,5S)-1-([1,1′-biphenyl]-4-ylcarbonyl)-5-[3-(2-hydroxyethyl)-1,2,4-oxadiazol-5-yl]-3-pyrrolidinone O-methyloxime,
(3Z,5S)-1-([1,1′-biphenyl]-4-ylcarbonyl)-5-[3-(2-hydroxyethyl)-1,2,4-oxadiazol-5-yl]-3-pyrrolidinone O-methyloxime,
(3E,5S)-5-[3-(2-hydroxyethyl)-1,2,4-oxadiazol-5-yl]-1-[(2′-methylbiphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime,
(3Z,5S)-5-[3-(2-hydroxyethyl)-1,2,4-oxadiazol-5-yl]-1-[(2′-methylbiphenyl-4-yl)carbonyl]pyrrolidin-3-one O-methyloxime,
(3EZ,5S)-1-([1,1′-biphenyl]-4-ylcarbonyl)-5-{5-[(dimethylamino)-methyl]-1,2,4-oxadiazol-3-yl}-3-pyrrolidinone O-methyloxime,
(3Z,5S)-1-([1,1′-biphenyl]-4-ylcarbonyl)-5-{5-[(dimethylamino)-methyl]-1,2,4-oxadiazol-3-yl}-3-pyrrolidinone O-methyloxime,
(3E,5S)-1-([1,1′-biphenyl]-4-ylcarbonyl)-5-{5-[(dimethylamino)-methyl]-1,2,4-oxadiazol-3-yl}-3-pyrrolidinone O-methyloxime,
(3EZ,5S)-5-{-5-[(dimethylamino)methyl]-1,2,4-oxadiazol-3-yl-}-1-[(2′-methylbiphenyl-4-yl)carbonyl]-pyrrolidin-3-one O-methyloxime,
(3Z,5S)-5-{5-[(dimethylamino)methyl]-1,2,4-oxadiazol-3-yl}-1-[(2′-methylbiphenyl-4-yl)carbonyl]-pyrrolidin-3-one O-methyloxime,
(3E,5S)-5-{5-[(dimethylamino)methyl]-1,2,4-oxadiazol-3-yl}-1-[(2′-methylbiphenyl-4-yl)carbonyl]-pyrrolidin-3-one O-methyloxime, and
(3Z/E, 5S)-1-(biphenyl-4-yl carbonyl)-5-hydroxymethyl)pyrrolidine-3-one-O-methyloxime.