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HRID 1887213作成日:2026年10月25日

Bromide ion → (S)-2-(2-benzyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)piperazin-1-yl)acetamide

https://huagongshe.com/reaction/1887213

反応式

関与物質

役割名称HCID仕込み量
反応物Bromide ionHCID 259—
反応物2-BromoacetamideHCID 69632—
反応物DiisopropylethylamineHCID 81531—
反応物(S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazineHCID 16725642—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-(2-benzyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)piperazin-1-yl)acetamideHCID 23627744—

反応条件

温度50 °C

反応手順

A solution of the bishydrochloride salt of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (Example 2) (110 mg, 0.25 mmol) in THF (2 mL) at room temperature was treated with diisopropylethylamine (165 μL, 1.0 mmol) followed by 2-bromoacetamide (42 mg, 0.3 mmol). The reaction mixture was heated at 50° C. for 8 h and an additional amount of bromide (42 mg, 0.3 mmol) then added. The reaction mixture was then stirred for an additional 16 h at room temperature and evaporated. The crude reaction was then partitioned between EtOAc (3 mL) and a saturated aqueous NaHCO3 solution (3 mL). The organic phase was isolated and further washed with an additional portion of a saturated aqueous NaHCO3 solution (3 mL) and brine (2×3 mL).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501745B2
出典データセットuspto-grants-2013_08
ORD IDord-ce866a58f98c42fbafb114a4d65c4b7a
出典メモuspto-grants-2013_08