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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533969생성일: 2026년 10월 25일

2-Phenylbutyric Acid → N-(7-Oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-2-phenyl-butyramide

https://huagongshe.com/reaction/533969

반응식

참여 물질

역할이름HCID투입량
반응물2-Phenylbutyric AcidHCID 7012—
반응물TriethylamineHCID 8471—
반응물2-Amino-4,5,6,7-tetrahydro-1,3-benzothiazol-7-oneHCID 587850—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물N-(7-Oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-2-phenyl-butyramideHCID 49718789—

반응 단계

2-Amino-5,6-dihydro-4H-benzothiazol-7-one (34 mg, 0.20 mmol) and 2-phenyl-butyric acid (33 mg, 0.20 mmol) were dissolved in N,N-dimethylformamide (1 mL) containing triethylamine (84.1 μL, 0.600 mmol). O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (84 mg, 0.22 mmol) was added and the solution was allowed to stir for 16 hours. The crude product was purified by reverse-phase preparative liquid chromatography (31 mg, 0.099 mmol, 49%). ESI-MS m/z calc. 314.1. found 315.3 (M+1)+ Retention time 2.90 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853415B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-392ee839301c49b2a1d5e281420b2b99
출처 메모uspto-grants-2014_10