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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1019955생성일: 2026년 10월 25일

3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylic acid → 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid {1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-3-morpholin-4-yl-propyl]-piperidin-4-yl}-amide

https://huagongshe.com/reaction/1019955

반응식

참여 물질

역할이름HCID투입량
반응물3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylic acidHCID 760993—
반응물2-Chloro-7-methoxyquinoxalineHCID 12686415—
반응물[1-(2-Mercapto-3-morpholin-4-yl-propyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 86662007—
생성물3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid {1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-3-morpholin-4-yl-propyl]-piperidin-4-yl}-amideHCID 66746407—

반응 단계

The title compound is prepared as a light brown lyophilizated powder following Scheme 3 and in analogy to Example 1 using 2-chloro-7-methoxy-quinoxaline, [1-(2-mercapto-3-morpholin-4-yl-propyl)-piperidin-4-yl]-carbamic acid tert-butyl ester and 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid as starting materials.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08716280B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-33443e5395c74e6aae6bd79d32fd3e2f
출처 메모uspto-grants-2014_05