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HRID 232727作成日:2026年10月27日

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

https://huagongshe.com/reaction/232727

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Amidosulfenyl chloride, N,N-dibutyl-HCID 81031—
反応物3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 18988349—
溶媒DichloromethaneHCID 6344—
生成物3,3a,4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-(dibutylaminosulfenyl)-2H-benz[g]indazole-2-carboxamideHCID 23359457—

反応手順

To a solution of the title compound of Step B (Example 1) (0.4 g, 0.96 mmol) in 8 ml methylene chloride cooled to 0° C. was added triethylamine (0.15 g) and dibutylaminosulfenylchloride (0.2 g). The reaction mixture was, warmed to room temperature and stirred for one hour. The mixture was subjected to silica gel column chromatography using hexane-ether (6:1) as the eluent. The title compound was obtained (0.24 g) in high purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591764
出典データセットuspto-grants-1997_01
ORD IDord-a077c5948d0f48569018d4e31e151f72
出典メモuspto-grants-1997_01