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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201124생성일: 2026년 10월 24일

(R)-tert-butyl 1-amino-1-oxo-3-(thiophen-2-yl)propan-2-ylcarbamate → (R)-2-amino-3-(thiophen-2-yl)propanamide

https://huagongshe.com/ko/reaction/2201124

반응식

참여 물질

역할이름HCID투입량
반응물(R)-tert-butyl 1-amino-1-oxo-3-(thiophen-2-yl)propan-2-ylcarbamateHCID 67776928—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물(R)-2-amino-3-(thiophen-2-yl)propanamideHCID 6750826932.5%

반응 단계

A solution of (R)-tert-butyl 1-amino-1-oxo-3-(thiophen-2-yl)propan-2-ylcarbamate (454 mg, 1.68 mmol) in TFA (4 mL) and CH2Cl2 (6 mL) was stirred at room temperature for 3 h. It was then concentrated in vacuo. The residue was partitioned between EtOAc and aq. 5% NaHCO3. The EtOAc phase was separated, washed with water, concentrated in vacuo to give (R)-2-amino-3-(thiophen-2-yl)propanamide (93 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359375B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-0985772c13014cd7bc7bbe25dc992065
출처 메모uspto-grants-2016_06