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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507839Generated: October 27, 2026

Ammonium Chloride → tert-Butyl (1(S)-(2-azido-1(S)-hydroxyethyl)-3(S)-{[2-(3-methoxypropoxy)benzoylamino]-methyl}4-methylpentyl)carbamate

https://huagongshe.com/reaction/507839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactanttert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-(R)-oxiranylpentyl)-carbamateHCID 86613450—
SolventMethanolHCID 887—
Producttert-Butyl (1(S)-(2-azido-1(S)-hydroxyethyl)-3(S)-{[2-(3-methoxypropoxy)benzoylamino]-methyl}4-methylpentyl)carbamateHCID 86613457—

Reaction Steps

The solution of 0.600 g of tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)—(R)-oxiranylpentyl)carbamate (Example 1b) in 12 ml of methanol is admixed with 0.208 g of sodium azide and 0.123 g of ammonium chloride, and stirred at reflux over 6 hours. The reaction solution is cooled, poured onto ice-water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) as a colourless oil. Rf=0.37 (2:1 EtOAc-heptane); Rt=18.95 (gradient II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786307B2
Source datasetuspto-grants-2010_08
ORD IDord-b0666a9316da45f09d37424ea70ca055
Source noteuspto-grants-2010_08