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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463941Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 131712193, compound

https://huagongshe.com/reaction/463941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 12882024HCID 12882024—
Reactant2-Methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetic acidHCID 54347340—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131712193HCID 13171219364.1%

Reaction Steps

Dicyclohexylcarbodiimide (0.99 g.) was added at ambient temperature to a solution of diphenylmethyl 7-amino-7-methoxy-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylate (2.1 g.) in dry tetrahydrofuran (20 ml.) and then 2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetic acid (syn isomer) (0.9 g) was added thereto at ambient temperature to give white precipitates. After stirring for 2 days at ambient temperature, the precipitates were filtered off and the filtrate was concentrated under reduced pressure to give brown oil. The oil as subjected to column chromatography on silica gel, eluted with a mixture of chloroform and ethyl acetate and the eluate was concentrated under reduced pressure to give diphenylmethyl 7-[2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetamido]-7-methoxy-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylate (syn isomer) (1.78 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544751
Source datasetuspto-grants-1985_10
ORD IDord-1b0a1b11fa7348beac2c8686ebbaff4c
Source noteuspto-grants-1985_10