Patent US6153928A successfully refreshed from Google Patents.
Patent US4347183A successfully refreshed from Google Patents.
US4347183A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Process for the synthesis of penems and carbapenems
Assignee: Merck Sharp & Dohme LLC
•
Filing: 1981-02-02
•
Granted: 1982-08-31
•
Expires: 2001-02-02
Abstract
Abstract Described is a novel process for the preparation of penems and carbapenems useful as antibacterial agents which comprises the reaction of an appropriate 4-substituted-azetidine-2-one with an acid halide in the presence of a tertiary amine and an alkaline earth metal carbonate, followed by reaction of the thereby formed 1-imido-4-substituted-azetidine-2-one with a trialkyl phosphite. Also described are novel penems useful as antibacterials which are prepared by the described process.
Inventors
- 👤 Adriano Afonso
- 👤 Frank Hon
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 12:24
CPC Classifications
C; C07; C07D; C07D499/00; C07D487/00; C07D487/02; C07D487/04; A; A61; A61P; A61P31/00; A61P31/04; C07D205/00; C07D205/02; C07D205/06; C07D205/08; C07D205/09; C07D477/00; C07D477/02; C07D477/04; C07D477/10; C07D477/12; C07D477/16; C07D477/22; C07D499/88; C07D503/00; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/18; C07F7/1804
Claims Analysis
Total Claims: 18
Claim 1
Independent Claim
229 words
The process for the preparation of a compound of Formula I: ##STR15## wherein R 1 is hydrogen, lower alkyl, acylamino or ##STR16## wherein R 4 is hydrogen, lower alkyl, aryl, heteroaryl and R 5 is an O-protecting group: R 2 is lower alkyl, aryl, alkylaryl, an N-protected amino-lower alkyl, an O-protected hydroxyalkyl, thioalkyl, thioaryl, thioheteroaryl, an α-(N-protected) amino acid ester or an alkylcarboxylic acid ester; R 3 is nitrile, tetrazole, or --COOR 6 wherein R 6 is lower alkyl, lower alkylthihalogenomethykl, aryl, allyl, or a metabolisable ester: X and Z are independently sulfur, oxygen, -NR 7 wherein R 7 is acyl, alkyl, aryl, or an N-protecting group; or --(CH 2 ) n --wherein n is 1 or 2; which comprises the reaction of an azetidinone of Formula A: ##STR17## wherein R 1 , R 2 , X and Z are as hereinabove defined, with an acid halide of Formula B: ##STR18## wherein in R 3 is as hereinabove defined, in an inert solvent in the presence of a tertiary amine and an alkaline earth metal carbonate; followed by reaction of the thereby produced imido derivative of Formula C: ##STR19## wherein in R 1 , R 2 , R 3 , X and Z are as hereinabove defined: with a trialkyl phosphite, said reaction being carried out at temperatures in the range of from about 20° to about 80° C.
Claim 2
Dependent Claim
229 words
The process for the preparation of a compound of Formula I: ##STR15## wherein R 1 is hydrogen, lower alkyl, acylamino or ##STR16## wherein R 4 is hydrogen, lower alkyl, aryl, heteroaryl and R 5 is an O-protecting group: R 2 is lower alkyl, aryl, alkylaryl, an N-protected amino-lower alkyl, an O-protected hydroxyalkyl, thioalkyl, thioaryl, thioheteroaryl, an α-(N-protected) amino acid ester or an alkylcarboxylic acid ester; R 3 is nitrile, tetrazole, or --COOR 6 wherein R 6 is lower alkyl, lower alkylthihalogenomethykl, aryl, allyl, or a metabolisable ester: X and Z are independently sulfur, oxygen, -NR 7 wherein R 7 is acyl, alkyl, aryl, or an N-protecting group; or --(CH 2 ) n --wherein n is 1 or 2; which comprises the reaction of an azetidinone of Formula A: ##STR17## wherein R 1 , R 2 , X and Z are as hereinabove defined, with an acid halide of Formula B: ##STR18## wherein in R 3 is as hereinabove defined, in an inert solvent in the presence of a tertiary amine and an alkaline earth metal carbonate; followed by reaction of the thereby produced imido derivative of Formula C: ##STR19## wherein in R 1 , R 2 , R 3 , X and Z are as hereinabove defined: with a trialkyl phosphite, said reaction being carried out at temperatures in the range of from about 20° to about 80° C.
Claim 3
Dependent Claim
18 words
The process of claim 1 including the subsequent step of isolating the thereby produced compound of formula I.
Claim 4
Dependent Claim
54 words
The process of claim 1 wherein to one mole of said azetidinone of formula A, there is added about a molar equivalent of each of said acid halide of formula B and said tertiary amine, at least a molar equivalent of said alkaline earth metal carbonate, and about two molar equivalents of trialkyl phosphite.
Claim 5
Dependent Claim
12 words
The process of claim 3 when carried out at about 60° C.
Claim 6
Dependent Claim
16 words
The process of claims 3 or 4 wherein said inert solvent is a halogeneated hydrocarbon solvent.
Claim 7
Dependent Claim
51 words
The process of claims 1 or 3 wherein said acid chloride of formula B is allyloxalyl chloride, said-tertiary amine is di-isopropylethylamine, said alkaline earth metal carbonate is calcium carbonate, said inert solvent is a halogenated hydrocarbon, and said trialkyl-phosphite is triethylphosphite, and said process is carried out at about 60° C.
Claim 8
Dependent Claim
28 words
The process of claim 6 wherein said azedtidinone is a compound of the following formula A": ##STR20## whereby is produced a compound of formula I" as follows: ##STR21##
Claim 9
Dependent Claim
23 words
The process of claim 7 wherein the azetidinone of formula A" is (3S, 4R, 5R)-3-[(1-trichlorethoxycarbonyloxyethyl)]-4-[(ethylthio) carbonothioylthio]azetidin-2-one whereby is produced allyl (5R, 6S, 8R)-6-(1-trichloroethoxycarbonyloxyethyl)-2-ethylthiopenem-3-carboxylate.
Claim 10
Dependent Claim
25 words
The process of claim 7 where in the azetidinone of formula A is (3S, 4R, 4R)-3-(1-trichlorethoxy-carbonyloxyethyl)-4-[(methylthio) carbonothioylthio] azetidin-2-one whereby is produced allyl (5R, 6S, 8R)-6-(1-trichloroethoxycarbonyloxy-2-methylthioethyl)penem-3-carboxylate.
Claim 11
Dependent Claim
173 words
The process for the preparation of a compound represented by formula I: ##STR22## wherein R 1 is hydrogen, lower alkyl, acylamino or ##STR23## wherein R 4 is hydrogen, lower alkyl, aryl or heteroaryl and R 5 is an O-protecting group: R 2 is lower alkyl, aryl, alkylaryl, an N-protected amino-lower alkyl, an O-protected hydroxyalkyl, thioalkyl, thioaryl, thioheteroaryl, an α-(N-protected) amino acid ester or an alkylcarboxylic acid esters R 3 is nitrile, tetrazole, or --COOR 6 wherein R 6 is lower alkyl, lower alkyltrihalogenomethyl, aryl, allyl, or a metabolisable ester; X and Z are independently sulfur, oxygen, --NR 7 --wherein R 7 is acyl, alkyl, aryl, or an N-protecting group; or 13 (CH 2 ) n --wherein n is 1 or 2; which comprises the reaction of an imido derivative of formual C: ##STR24## wherein R 1 , R 2 , R 3 , X and Z are as hereinabove defined; with a trialkyl phosphite, said reaction being carried out at temperatures in the range of from about 20° C. to about 80° C.
Claim 12
Dependent Claim
173 words
The process for the preparation of a compound represented by formula I: ##STR22## wherein R 1 is hydrogen, lower alkyl, acylamino or ##STR23## wherein R 4 is hydrogen, lower alkyl, aryl or heteroaryl and R 5 is an O-protecting group: R 2 is lower alkyl, aryl, alkylaryl, an N-protected amino-lower alkyl, an O-protected hydroxyalkyl, thioalkyl, thioaryl, thioheteroaryl, an α-(N-protected) amino acid ester or an alkylcarboxylic acid esters R 3 is nitrile, tetrazole, or --COOR 6 wherein R 6 is lower alkyl, lower alkyltrihalogenomethyl, aryl, allyl, or a metabolisable ester; X and Z are independently sulfur, oxygen, --NR 7 --wherein R 7 is acyl, alkyl, aryl, or an N-protecting group; or 13 (CH 2 ) n --wherein n is 1 or 2; which comprises the reaction of an imido derivative of formual C: ##STR24## wherein R 1 , R 2 , R 3 , X and Z are as hereinabove defined; with a trialkyl phosphite, said reaction being carried out at temperatures in the range of from about 20° C. to about 80° C.
Claim 13
Dependent Claim
75 words
The process of claim 10 wherein the compound represented by Formula C is prepared by the reaction of an azetidinone represented by Formula A: ##STR25## wherein R 1 , R 2 , X and Z are as defined in claim 13, with an acid halide represented by Formula B: ##STR26## wherein R 3 is as defined in claim 13; in an inert solvent in the presence of a tertiary amine and alkaline earth metal carbonate.
Claim 14
Dependent Claim
9 words
The process of claim 10 wherein X is sulfur.
Claim 15
Dependent Claim
9 words
The process of claim 10 wherein X is oxygen.
Claim 16
Dependent Claim
18 words
The process of claim 10 wherein X is ##STR27## and R 7 is as defined in claim 13.
Claim 17
Dependent Claim
20 words
The process of claim 10 wherein X is --(CH 2 ) n --and n is as defined in claim 10.
Claim 18
Dependent Claim
18 words
The process of claim 15 wherein n is 1, Z is sulfur, and R 2 is N-protected aminoethyl.
References Cited (Backward Citations)
GB1455016A
Cited
US4293599A
Cited
US4172899A
Cited
GB1591438A
Cited
GB2013674A
Cited
US4203902A
Cited
US4206219A
Cited
GB2045236A
Cited
GB2045235A
Cited
GB2046746A
Cited
US4269771A
Cited
GB2066249A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1985-08-30 | 1986-03-01 | 1986-08-31 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1989-08-30 | 1990-03-01 | 1990-08-31 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1993-08-30 | 1994-03-01 | 1994-08-31 | $7700.00 | Window Closed / Lapsed |