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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183039Generated: October 29, 2026

HCID 22480752, compound → Tert-butyl 3-aminoazetidine-1-carboxylate

https://huagongshe.com/reaction/2183039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22480752HCID 22480752—
SolventMethanolHCID 887—
SolventMethylamineHCID 6329—
ProductTert-butyl 3-aminoazetidine-1-carboxylateHCID 1516507—

Reaction Steps

A solution of tert-butyl 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-azetidinecarboxylate (Preparation 77) in methylamine in methanol (2M) (10 ml) was stirred in a sealed tube at 55° C. for 3 hours. On cooling a precipitate formed and the reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (100 ml) and washed with water (100 ml, containing (2M) hydrochloric acid (3 ml)) and water (50 ml, containing (2M) hydrochloric acid (2 ml)). The combined aqueous was basified with (2M) sodium hydroxide solution (20 ml) and extracted with ethyl acetate (3×75 ml). The combined organic layers were dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a gradient system of 97.5:2.5:0.25 (dichloromethane:methanol:ammonia) gradually changing to 90:10:1 (dichloromethane:methanol:ammonia) to afford the title compound (935 mg) of approximately 90% purity, which was used in preparation without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897306B2
Source datasetuspto-grants-2005_05
ORD IDord-16d73c9c5f2f489ba93f15ff768d65f5
Source noteuspto-grants-2005_05