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HRID 386528作成日:2026年10月25日

1-(5-Trifluoromethyl-pyridin-2-yl)-piperazine → (2S)-2-{4-[5-(Trifluoromethyl)pyridin-2-yl]piperazin-1-yl}propanoic acid

https://huagongshe.com/reaction/386528

反応式

関与物質

役割名称HCID仕込み量
反応物1-(5-Trifluoromethyl-pyridin-2-yl)-piperazineHCID 667618—
反応物(2R)-2-Bromopropanoic acidHCID 6992152—
溶媒DichloromethaneHCID 6344—
生成物(2S)-2-{4-[5-(Trifluoromethyl)pyridin-2-yl]piperazin-1-yl}propanoic acidHCID 66628464—

反応条件

温度35 °C

反応手順

A solution of 1-(5-trifluoromethyl-pyridin-2-yl)-piperazine (2.77 g, 11.99 mmoles) in DCM (42 mL) and TEA (4.2 mL) was treated with (2R)-2-bromo-propionic acid (1.19 mL, 13.2 mmoles) and stirred overnight at 35° C. The DCM was removed under reduced pressure to provide crude title compound as a yellowish solid that was used in the next step. MS(APCI+) m/z 304 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372841B2
出典データセットuspto-grants-2013_02
ORD IDord-d7a3a3a4e5fa4375861b0c7d2c02bfee
出典メモuspto-grants-2013_02