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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231504Generated: October 31, 2026

N,N-Dimethylaniline → HCID 131715767, compound

https://huagongshe.com/reaction/2231504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantBenzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylateHCID 13239626—
ReactantHCID 54194454HCID 54194454—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 131715767HCID 131715767—

Reaction Steps

2.12 g (3 mmol) of 2-(1-benzhydryloxycarbonyl-1-cyclopentyloxyimino)-2-(2-tritylaminothiazol-4-yl)acetic acid (syn-isomer) and 1.24 g (3 mmol) of benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate were dissolved in 50 ml of methylene chloride, and 1.2 ml (9.6 mmol) of N,N-dimethylaniline was added thereto under cooling with ice. Then, 0.29 ml (3.15 mmol) of phosphorus oxychloride was dropwise added thereto and the reaction solution was stirred at the same temperature for 4 hours. To the reaction solution, 30 ml of chloroform and 30 ml of water were added. The organic layer was washed with water and a saturated sodium chloride aqueous solution, then dried over anhydrous sodium sulfate and concentrated to obtain benzhydryl 7-[2-(1-benzhydryloxycarbonyl-1-cyclopentyloxyimino)-2-(2-tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate (syn-isomer), which was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782155
Source datasetuspto-grants-1988_11
ORD IDord-d025573ceae048bbaf1ece30284bc1ed
Source noteuspto-grants-1988_11