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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200297Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 16166018, compound

https://huagongshe.com/reaction/1200297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 13821813HCID 13821813—
ReactantHCID 14050777HCID 14050777—
SolventDichloromethaneHCID 6344—
ProductHCID 16166018HCID 16166018—

Reaction Steps

To an ice-cooled solution of the crude product obtained in Step 5 (5.6 g) and (6R,7R)-7-amino-3-[(2-diphenylmethyloxycarbonyl-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester (5.0 g) in dichloromethane (170 ml) was added dicyclohexylcarbodiimide (1.4 g), and the mixture was stirred at room temperature for five hours. After filtering off the insoluble matters, the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the insoluble matters were filtered off. The filtrate was washed with brine and dried over anhydrous sodium sulfate. The dried solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography, giving 0.73 g (less polar form) and 1.39 g (more polar form) of the objective compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904791
Source datasetuspto-grants-1990_02
ORD IDord-1ee9aae6190740d4878d7434ea8a494f
Source noteuspto-grants-1990_02