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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232726생성일: 2026년 10월 26일

Triethylamine → 3,3a, 4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-(1-methylpropoxycarbonylsulfenyl)-2H-benz[g]indazole-2-carboxamide

https://huagongshe.com/reaction/232726

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(1-Methylpropoxycarbonyl)sulfenyl chlorideHCID 13633290—
반응물3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 18988349—
용매DichloromethaneHCID 6344—
생성물3,3a, 4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-(1-methylpropoxycarbonylsulfenyl)-2H-benz[g]indazole-2-carboxamideHCID 18988348—

반응 조건

온도0 °C

반응 단계

To a solution of the title compound of Step B (Example 1) (0.4 g, 0.96 mmol) in 5 ml methylene chloride was added triethylamine (0.12 g) and cooled to 0° C. To this solution was added (1-methylpropoxycarbonyl)sulfenyl chloride (Step A) (0.2 g, 0.0012 mol). The mixture was stirred at room temperature for one hour. At this stage thin layer chromatography indicated only partial conversion, therefor, addition- al amounts of (1-methylpropoxycarbonyl)sulfenyl chloride (0.2 g) and triethylamine (0.12 g) was added and the mixture was let stand overnight. The reaction mixture was subjected to silica gel column chromatography using hexane-ether (7:1) as eluent. The title compound was obtained (0.22 g) in high purity; m.p.: 125°-126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591764
출처 데이터셋uspto-grants-1997_01
ORD IDord-d577324eba2447b3986e4aa88efcf673
출처 메모uspto-grants-1997_01