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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1259834생성일: 2026년 10월 27일

6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one → 6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-one

https://huagongshe.com/reaction/1259834

반응식

참여 물질

역할이름HCID투입량
반응물6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 2763681—
반응물(S)-Glycidoxy-t-butyldimethylsilaneHCID 10954307—
용매AcetonitrileHCID 6342—
생성물6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-oneHCID 6673769549.5%

반응 조건

온도50 °C

반응 단계

To a solution of tert-butyl-dimethyl-((S)-1-oxiranylmethoxy)-silane (commercial; 13.0 g, 69 mmol) in MeCN (220 mL) was added LiClO4 (22 g, 207 mmol). 6-amino-4H-benzo[1,4]oxazin-3-one (commercial; 11.45 g, 64 mmol) was added and the mixture was stirred at 50° C. for 6 h. The solvent was removed in vacuo and the residue was purified by CC (DCM/MeOH/NH4OH 1000/25/2 to 1000/100/2) to afford the title intermediate as a pale brown foam (11.16 g, 44% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466168B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-9ed9890e33ac4d40be18c75db3f7c8bd
출처 메모uspto-grants-2013_06