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HRID 471048作成日:2026年10月27日

Ethyl bromodifluoroacetate → tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/471048

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromodifluoroacetateHCID 69585—
反応物tert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 23396319—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylateHCID 57988980—

反応条件

温度20 °C

反応手順

A solution of tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate (1.702 g) in DMF (20 mL) at 20° C. was treated with ethyl 2-bromo-2,2-difluoroacetate (1.5 g) and the mixture stirred for 90 minutes at 20° C. under nitrogen. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure to afford the subtitled compound. Yield 2.5 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629271B2
出典データセットuspto-grants-2014_01
ORD IDord-435b4c8bbeae44fe81601b8d05ad124c
出典メモuspto-grants-2014_01