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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851586Generated: October 26, 2026

Triethylamine → 2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]-amino-3-cephem-4-carboxylate

https://huagongshe.com/reaction/851586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2,2,2-Trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochlorideHCID 12834135—
ReactantN-(1-cyclopropylethoxycarbonyl)phenylglycineHCID 53938438—
CatalystN,N-DimethylbenzylamineHCID 7681—
SolventDichloromethaneHCID 6344—
Product2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]-amino-3-cephem-4-carboxylateHCID 13171299488.2%

Reaction Steps

A solution of N-(1-cyclopropylethoxycarbonyl)-phenylglycine (1.63 g), triethylamine (0.60 g) and dimethylbenzylamine (2 drops) in dried dichloromethane (10 ml) was dropwise added at -10° C. to a solution of ethyl chloroformate (0.67 g) in dried dichloromethane (15 ml), and the mixture was stirred for 1 hour. The mixture was cooled at -10° to 15° C. and to the mixture was dropwise added over 10 minutes a solution of 2,2,2-trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochloride (2.2 g) and triethylamine (0.55 g) in dried dichloromethane (20 ml), after which the mixture was stirred for 2.5 hours at the same temperature. After the reaction, the reaction mixture was in turn washed with water, 2% hydrochloric acid, a saturated sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution and then dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was pulverized by adding isopropyl ether, after which the powder was collected by filtration and dried to give 2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]-amino-3-cephem-4-carboxylate (3.0 g), mp 165° to 167.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04385176
Source datasetuspto-grants-1983_05
ORD IDord-8c5da565f35c49d48c31e19db902c188
Source noteuspto-grants-1983_05