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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2396082생성일: 2026년 10월 27일

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/2396082

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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, additional amounts of (1-methylpropoxycarbonyl)sulfenyl chloride (0.2 g) and triethylamine (0.12g) was added and the mixture was let stand over night. The reaction mixturewas subjected to silica gel column chromatography using hexane-ether (7:1) as eluent. The title compound was obtained (0 g) in high purity; m.p.: 125°-126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05491162
출처 데이터셋uspto-grants-1996_02
ORD IDord-b685eade98604f9f8ba3bb9586b70bbd
출처 메모uspto-grants-1996_02