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HRID 29189作成日:2026年10月26日

Isopropanol → tert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamate

https://huagongshe.com/reaction/29189

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物DiisopropylethylamineHCID 81531—
反応物O-tert-butylhydroxylamine hydrochlorideHCID 2777906—
反応物(1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamateHCID 20638362—
生成物tert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamateHCID 59090702—

反応手順

tert-Butyl-N-((1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamate (0.155 g, 0.59 mmol) and O-(tert-butyl)hydroxylamine hydrochloride (0.089 g, 0.71 mmol) were heated with diisopropylethylamine (0.154 ml, 0.88 mmol) in isopropanol (2 ml) in a sealed tube at 60° C. for 5 days. The reaction mixture was concentrated in vacuo, taken up in EtOAc, washed with sat. aq. NaHCO3, and brine. The organic phase was dried over MgSO4, filtered and solvent removed in vacuo. Purication by column chromatography (1% MeOH in CH2Cl2) gave 100 mg of a white solid which was used directly in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419967B2
出典データセットuspto-grants-2008_09
ORD IDord-52b8f8f029684768afcaa2b5b52f915e
出典メモuspto-grants-2008_09