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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065196Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 131712713, compound

https://huagongshe.com/reaction/1065196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant18820-83-2HCID 312731—
ReactantHCID 12884459HCID 12884459—
ReactantHCID 54174508HCID 54174508—
SolventDimethylformamideHCID 6228—
ProductHCID 131712713HCID 131712713—

Reaction Conditions

Temperature16 °C

Reaction Steps

A mixture of 1.69 g of the product of Step A, 0.685 g of pyridine hydroiodide, 1.16 g of benzhydryl 3-acetoxymethyl-7-amino-ceph-3-eme-4-carboxylate and 1.36 g of dicyclohexylcarbodiimide was admixed with 17 ml of dimethylformamide and the mixture was cooled to 16° C. for 30 minutes and was then vacuum filtered. 400 ml of ether were added to the filtrate and the mixture was stirred for 5 minutes and allowed to stand for one hour. The mixture was decanted and the gum was washed with ether and was added to 50 ml of ether. The mixture was kneaded until concretization and was vacuum filtered. The product was washed with ether and dried to obtain 1.92 of raw product which was chromatographed over silica gel. Elution with a 91-9 chloroform-acetonitrile mixture yielded 790 mg of amorphous syn isomer of benzhydryl 3-acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-(2-thiocyanatoethoxyimino)-acetamido]-ceph-3-eme-4-carboxylate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328225
Source datasetuspto-grants-1982_05
ORD IDord-b122df6a29ac40df8fffce779d280384
Source noteuspto-grants-1982_05