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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078125Generated: November 4, 2026

Acetic Anhydride → 2-(Acetylamino)-4-(t-butyloxycarbonylamino)-1,5-diphenyl-3-hydroxypentane

https://huagongshe.com/reaction/1078125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-2-(t-butyloxycarbonylamino)-1,5-diphenyl-3-hydroxypentaneHCID 14704377—
SolventDichloromethaneHCID 6344—
Product2-(Acetylamino)-4-(t-butyloxycarbonylamino)-1,5-diphenyl-3-hydroxypentaneHCID 22910278—

Reaction Steps

A solution of 20 mg of the resultant compound of Example 11 and 0.05 ml of triethylamine in 1 ml of dichloromethane was cooled to 0° C. and treated with 0.01 ml of acetic anhydride. After 30 min, the solution was partitioned between water and dichloromethane, and the organic phase was dried over Na2SO4 and concentrated to give 23 mg (100%) of the desired compound (Rf 0.5, 10% methanol in chloroform). Mass spectrum: (M+H)+ =413.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545750
Source datasetuspto-grants-1996_08
ORD IDord-12f80abcf1bc473bbe6a846ddc5fcb7c
Source noteuspto-grants-1996_08