戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1393009作成日:2026年10月26日

Triethylamine → Ethanesulfonic acid methyl-(2,3,11a-trimethyl-2,3,3a,4,5,5a,5b,6,8,9,10,11,11a,11b,12,13-hexadecahydro-1H-2-aza-pentaleno[1,6a-a]phenanthren-9-yl)-amide

https://huagongshe.com/reaction/1393009

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethanesulfonyl chlorideHCID 11667—
反応物KurchineHCID 551434—
溶媒DichloromethaneHCID 6344—
生成物Ethanesulfonic acid methyl-(2,3,11a-trimethyl-2,3,3a,4,5,5a,5b,6,8,9,10,11,11a,11b,12,13-hexadecahydro-1H-2-aza-pentaleno[1,6a-a]phenanthren-9-yl)-amideHCID 6742427782%

反応手順

A mixture of compound 7B (15 mg, 0.044 mmol), ethanesulfonyl chloride (5 μL, 1.5 eq), triethylamine (15 μL, 3.0 eq) and dichloromethane (1 mL) was stirred at room temperature overnight. The clear solution was directly loaded on silica gel column and eluted with 0.5% ammonium hydroxide and 5% methanol in dichloromethane to give the desired product (12.5 mg, 82% yield)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07345034B2
出典データセットuspto-grants-2008_03
ORD IDord-2874a8859d944740ba71f44972c9b5d7
出典メモuspto-grants-2008_03