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HRID 1614151作成日:2026年10月26日

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

https://huagongshe.com/reaction/1614151

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 18988349—
反応物Ethyl (chlorosulfenyl)(1-methylethyl)carbamateHCID 20139494—
溶媒DichloromethaneHCID 6344—
生成物3,3a, 4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-[N'-(1-methylethyl)-N'-(ethoxycarbonyl)aminosulfenyl]-2H-benz[g]indazole-2-carboxamideHCID 8839671585.7%

反応手順

To a solution of the title compound of Step B (2.0 g, 4.8 mmol) in 50 ml methylene chloride cooled to 0° C. was added triethylamine (1.0 g, 0.01 mol) and ethyl (chlorosulfenyl)(1-methylethyl)carbamate from Step D (1.4 g, 7.7 mmol). The mixture was allowed to warm to room temperature and stirred for one hour. The crude mixture was purified by silica column chromatography using ether-hexane (1:2) as eluent. The title compound (2.38 g) was obtained in about 90% purity (mp: 130°-134°). Extraction of the product with ether-hexane (2:1) gave 1.8 g of a highly pure material mp: 139°-140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05196408
出典データセットuspto-grants-1993_03
ORD IDord-cd5e9a4d26844e49bf100448687b566e
出典メモuspto-grants-1993_03