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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904152Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 131713478, compound

https://huagongshe.com/reaction/1904152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant18820-83-2HCID 312731—
ReactantHCID 12884459HCID 12884459—
ReactantHCID 54498501HCID 54498501—
SolventDimethylformamideHCID 6228—
ProductHCID 131713478HCID 131713478—

Reaction Steps

A solution of 1 g of the product of Step A, 0.38 g of pyridine hydroiodide, 0.63 g of dicyclohexylcarbodiimide, 0.60 g of benzhydryl 3-acetoxymethyl-7-amino-ceph-3-eme-4-carboxylate and 5 ml of anhydrous dimethylformamide was stirred at room temperature for 30 minutes and was vacuum filtered to remove dicyclohexylurea. 100 ml of ether were added to the filtrate and the mixture was stirred for 10 minutes and was vacuum filtered. The product was rinsed with ether and was chromatographed over silica gel. Elution with a 7-1 ethyl acetate-ethanol mixture yielded 0.524 g of the syn isomer of benzhydryl 3-acetoxymethyl-7-[2-2tritylamino-4-thiazolyl)-2-(2-morpholinoethoxyimino)-acetamido]-ceph-3-eme-4-carboxylate hydroiodide melting at 167° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04439433
Source datasetuspto-grants-1984_03
ORD IDord-31c3df6b5a46432d843d10570b5129a2
Source noteuspto-grants-1984_03