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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379384Generated: October 31, 2026

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

https://huagongshe.com/reaction/1379384

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 numberUS05670675
Source datasetuspto-grants-1997_09
ORD IDord-27be687a0aad419bae2bf0f89e802c9d
Source noteuspto-grants-1997_09