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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64289생성일: 2026년 10월 25일

Triethylamine → tert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/64289

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylateHCID 21306970127.9%

반응 단계

To a solution of 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid (5.15 g, 25.6 mmol) in THF (100 mL) was added DCC (7.11 g, 34.5 mmol), Et3N (5.18 g, 51.2 mmol) and N,O-dimethylhydroxylamine hydrochloride (3.44 g, 35.3 mmol), the reaction was stirred at RT for about 16 hr. Concentrated under reduced pressure to remove solvent, the residue was portioned between EA (100 mL) and water (50 mL), the aqueous was further extracted with EA (50 mL×3). The combined organic phases were washed with brine (20 mL), concentrated under reduced pressure to remove solvent, then purified by column chromatography on silica gel (200-300 mesh, CH2Cl2/MeOH=20/1) to give the crude product (˜8.0 g) as a colorless oil. MS (ESI) m/e [M+23]+ 266.9, [M−55]+ 189.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447106B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-06856d51830f42eebc70c84fb7bd2dd1
출처 메모uspto-grants-2016_09