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HRID 456574作成日:2026年10月25日

Sodium Hydroxide → 1-[2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-yl]-ethyl]-cyclopropanecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/456574

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazineHCID 11289155—
反応物Tert-Butyl 1-(2-oxoethyl)cyclopropanecarboxylateHCID 58817571—
溶媒DichloromethaneHCID 6344—
生成物1-[2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-yl]-ethyl]-cyclopropanecarboxylic acid tert-butyl esterHCID 5881761591.2%

反応手順

To a solution of 4.2 g (14.7 mmol) of 1-(6-trifluoromethyl-benzo[b]thiophen-3-yl)-piperazine in 100 mL of dichloromethane under nitrogen was added 3.5 g (19.1 mmol) of 1-(2-Oxo-ethyl)-cyclopropanecarboxylic acid tert-butyl ester. After stirring 10 minutes at room temperature 6.5 g (30.7 mmol) of sodium triacetoxyborohydride was added portion-wise. After 30 minutes 100 mL of 0.5 N aqueous sodium hydroxide was added and the reaction was stirred for 15 minutes. The organic layer was separated, dried and concentrated to deliver a paste. This was taken up in methanolic hydrogen chloride. The salt thus obtained was recrystallized from ethyl acetate/methanol to deliver 6.6 g (13.4 mmol) of the desired product as a white powder mp=187–9° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07186724B2
出典データセットuspto-grants-2007_03
ORD IDord-74ed5fa610a44a098ebf7be81fd80903
出典メモuspto-grants-2007_03