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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527951생성일: 2026년 10월 25일

6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-one → (RS)-6-[4-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-butylamino]-4H-benzo[1,4]thiazin-3-one

https://huagongshe.com/reaction/527951

반응식

참여 물질

역할이름HCID투입량
반응물6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-oneHCID 686901—
반응물(R)-tert-butyldimethyl(2-(oxiran-2-yl)ethoxy)silaneHCID 11030897—
용매Water ethanolHCID 19096565—
생성물(RS)-6-[4-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-butylamino]-4H-benzo[1,4]thiazin-3-oneHCID 6722262329%

반응 단계

A solution of 6-amino-4H-benzo[1,4]thiazin-3-one (3.56 g, 19.8 mmol; commercial) and (RS)-tert-butyl-dimethyl-(2-oxiranyl-ethoxy)-silane (prepared according to J. Org. Chem. (2008), 73, 1093; 4.0 g, 19.8 mmol) in EtOH/H2O (9:1; 140 mL) was heated at 80° C. for 2 days. The mixture was concentrated under reduced pressure and the residue was purified by CC (DCM/MeOH/NH4OH 1000:50:4) to afford the title intermediate as a brown oil (2.20 g, 29% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346804B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-587ada34a0fd451b928f5a12f59fd650
출처 메모uspto-grants-2016_05