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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850897Generated: October 31, 2026

Ethylmorpholine → HCID 54201682, compound

https://huagongshe.com/reaction/850897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54062324HCID 54062324—
SolventDichloromethaneHCID 6344—
ProductHCID 54201682HCID 54201682—

Reaction Steps

0.5 ml of N-ethylmorpholine and 0.37 ml of acetic anhydride were added in sequence to a solution of 1.95 g of N-[N-[N-[N-(O-tert-butyl-L-seryl)-D-valyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucine benzyl ester in 70 ml of anhydrous dichloromethane. The mixture was stirred at room temperature for 1 hour and was then washed in sequence with 5% aqueous citric acid solution, saturated aqueous sodium bicarbonate solution and saturated brine. The organic phase was dried over anhydrous magnesium sulphate and evaporated. Chromatography of the residue on silica using 5% methanol in dichloromethane for the elution gave afforded 1.45 g of N-[N-[N-[N-(N-acetyl-O-tert-butyl-L-seryl)-D-valyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucine benzyl ester; MS: m/e 780.6 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018020
Source datasetuspto-grants-2000_01
ORD IDord-329ddc7e71454b478dbc83d4b1b08bbc
Source noteuspto-grants-2000_01