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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633807생성일: 2026년 10월 26일

1-Hydroxybenzotriazole → HCID 178487804, 화합물

https://huagongshe.com/reaction/633807

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylic acidHCID 760993—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물HCID 178487802HCID 178487802—
용매DimethylformamideHCID 6228—
생성물HCID 178487804HCID 178487804—

반응 단계

3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid (31 mg, 0.14 mmol, 1.0 eq) is added at room temperature to a stirred solution of trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexylamine (47 mg, 0.14 mmol, 1.0 eq) in N,N-dimethylformamide (4 mL), followed by 1-hydroxybenzotriazole (24 mg, 0.16 mmol, 1.1 eq), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (32 mg, 0.16 mmol, 1.15 eq) and N,N-diisopropylethylamine (56 μL, 0.32 mmol, 2.25 eq). After 15 hours stirring at room temperature, solvent is evaporated and the residue is extracted with dichloromethane (3×10 mL) and water (10 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a crude product that is purified by preparative HPLC to afford 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid [trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexyl]-amide as a white lyophilized powder (16 mg, 21% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321788B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-9c7b61a897544325ac4f7c0220166143
출처 메모uspto-grants-2016_04