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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603648Generated: October 26, 2026

Dicyclohexylcarbodiimide → N-(6-phenylhexyl)-(4-benzylthio-2-oxoazetidin-1-yl)acetamide

https://huagongshe.com/reaction/1603648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Phenylhexan-1-amineHCID 145558—
Reactant(4-Benzylthio-2-oxoazetidin-1-yl)acetic acidHCID 19605256—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(6-phenylhexyl)-(4-benzylthio-2-oxoazetidin-1-yl)acetamideHCID 1960528170%

Reaction Steps

A solution of 6-phenylhexylamine (Morse M. A. et al., Cancer Research, 1991, 1846), (7.0 g, 40 mmol) in DMF (20 ml) was added to DCC (8.2 g, 40 mmol), hydroxybenzotriazole (5.3 g, 39 mmol) and (4-benzylthio-2-oxoazetidin-1-yl)acetic acid (10 g, 39 mmol) and the mixture stirred for 2 hours at room temperature. Ethyl acetate (250 ml) was added, the precipitate filtered, the filtrate washed with dil NaHCO3, water (×2), dried (MgSO4) and evaporated to an oil which was purified by flash chromatography on silica gel using hexane/ethyl acetate (1:1). Evaporation of the appropriate fractions followed by treatment with hexane gave a white solid (11.2 g, 70%), mp 65-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-c9fa6819c6a942b5909480318dede038
Source noteuspto-grants-1999_11