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HRID 457842作成日:2026年10月26日

4-(5-methoxy-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl ester → 4-[5-methoxy-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/457842

反応式

関与物質

役割名称HCID仕込み量
反応物4-(5-methoxy-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl esterHCID 11335656—
反応物3-Thiopheneethanol methanesulfonateHCID 14422934—
生成物4-[5-methoxy-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidine-1-carboxylic acid ethyl esterHCID 6941282557%

反応手順

This compound was prepared following the procedure described in example 13 (part B) starting with 8.7 g (28.6 mmol) of 4-(5-methoxy-1H-indol-3-yl)-piperidine-1-carboxylic acid ethyl ester and 6.9 g (33.4 mmol) of 2-thiophen-3-yl-ethyl methanesulfonate. The reaction mixture was stirred at room temperature for 18 hours. After standard work-up, 6.7 g (57% of yield) of 4-[5-methoxy-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidine-1-carboxylic acid ethyl ester were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189741B2
出典データセットuspto-grants-2007_03
ORD IDord-1fa16d2b677e49238a038546da9c7e56
出典メモuspto-grants-2007_03