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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607415Generated: October 30, 2026

4-Methylmorpholine → HCID 178501400, compound

https://huagongshe.com/reaction/1607415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDi(succinimido) carbonateHCID 676246—
ReactantHCID 57214422HCID 57214422—
ReactantHCID 178419105HCID 178419105—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 178501400HCID 17850140073.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 330 mg of 2-benzylidene-3-(1-naphthylmethylcarbamoyl)propionic acid, 260 mg of N,N'-disuccinimidylcarbonate and 1 ml of pyridine in 20 ml of dry acetonitrile was stirred for 3 hour at room temperature. The solution was added to a solution of 300 mg of L-histidine methyl ester dihydrochloride and 150 mg of N-methylmorpholine in 20 ml of dry N,N-dimethylformamide, and the mixture was stirred for 16 hours at 40° C. The reaction mixture was concentrated under reduced pressure, and a 5% aqueous sodium bicarbonate solution was added to the residue. The precipitates were collected by filtration to obtain 350 mg of N-[2-benzylidene-3-(1-naphthylmethylcarbamoyl)propionyl]-L-histidine methyl ester as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863904
Source datasetuspto-grants-1989_09
ORD IDord-31e9289029fe4c73b7d5836dcdb84c4c
Source noteuspto-grants-1989_09