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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607413Generated: October 29, 2026

Dichloromethane → HCID 178445899, compound

https://huagongshe.com/reaction/1607413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(+/-)-2-(1-Naphthylmethylcarbamoyl)-3-phenylpropionic acidHCID 14600096—
ReactantHCID 178445905HCID 178445905—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178445899HCID 17844589912.6%

Reaction Steps

A mixture of 102 mg of (±)-2-(1-naphthylmethylcarbamoyl)-3-phenylpropionic acid and 50 mg of 1,1'-carbonyldiimidazole was added to 5 ml of dichloromethane, and the mixture was stirred for 40 minutes at room temperature. The reaction mixture was added to a solution of 202 mg of L-histidyl-L-leucinal semicarbazone.2p-toluenesulfonic acid salt and 0.09 ml of triethylamine in 3 ml of N,N-dimethylformamide, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and a 5% aqueous sodium bicarbonate solution was added to the residue. The mixture was extracted with ethyl acetate, dried and concentrated under reduced pressure. The residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume) to obtain 24 mg of N-[(±)-2-(1-naphthylmethylcarbamoyl)-3-phenylpropionyl]-L-histidyl-L-leucinal semicarbazone as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863904
Source datasetuspto-grants-1989_09
ORD IDord-78f84b598104434f95eb0143dd5f708c
Source noteuspto-grants-1989_09