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HRID 1786459作成日:2026年10月26日

tert-Butyl piperazine-1-carboxylate → [6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/1786459

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Cyclopropanesulfonyl chlorideHCID 2760919—
反応物1-(Cyclopropylsulfonyl)piperazineHCID 45496790—
反応物6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid hydrochlorideHCID 67017930—
生成物[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanoneHCID 6856678162%

反応手順

The title compound was synthesized in analogy to example 1, from 6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid hydrochloride (example 1, intermediate a) and cyclopropylsulfonyl-piperazine (prepared in analogy to International Patent Application Publ. No. WO 2003/064413 by using cyclopropylsulfonyl chloride and tert-butyl 1-piperazinecarboxylate) to afford the title compound as a light-yellow solid (62%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07507736B2
出典データセットuspto-grants-2009_03
ORD IDord-2200d6b7e9f94cecbba6c389b32d518b
出典メモuspto-grants-2009_03