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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371672Generated: October 29, 2026

Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate → HCID 88485747, compound

https://huagongshe.com/reaction/2371672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylateHCID 13239626—
ReactantHCID 88485782HCID 88485782—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 88485747HCID 8848574741.2%

Reaction Steps

To a solution of diphenylmethyl 7-amino-3-chloromethyl-3-cephem-4-carboxylate (VIa) (685 mg, 1.65 mmol) in THF (8.3 ml) was added benzotriazol-1-yl 2-(2-aminothiazol-4-yl)-2-(Z)-(diphenylmethyloxycarbonyl-(3,4-dihydroxyphenyl) methyl]oxyiminoacetate (IIIa) (955 mg, 1.50 mmol) and the mixture was stirred for 5 hr at room temperature. The reaction mixture was diluted with ethyl acetate, washed with water dried over MgSO4 and concentrated under reduced pressure. The crude product was chromatographed on a column of silica gel to afford 566 mg (41% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05095012
Source datasetuspto-grants-1992_03
ORD IDord-7fb334608921474e8d0b5478523812fc
Source noteuspto-grants-1992_03