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HRID 572210作成日:2026年10月26日

Acetic Acid → 6-chloro-N-[(1S)-1-(3-{[1-(3-methylphenyl)ethyl]amino}phenyl)ethyl]pyrazin-2-amine

https://huagongshe.com/reaction/572210

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrochloric AcidHCID 313—
反応物1-(5-Methylpyridin-3-yl)ethan-1-oneHCID 577569—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(S)-N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amineHCID 25218447—
溶媒1,2-DichloroethaneHCID 11—
生成物6-chloro-N-[(1S)-1-(3-{[1-(3-methylphenyl)ethyl]amino}phenyl)ethyl]pyrazin-2-amineHCID 8753303214.2%

反応条件

温度80 °C

反応手順

To a solution of 1-(5-methylpyridin-3-yl)ethanone (135 mg, 1 mmol) and N-[(1S)-1-(3-aminophenyl)ethyl]-6-chloropyrazin-2-amine (248 mg, 1 mmol) in 1,2-dichloroethane (5 mL) was added sodium triacetoxyborohydride (300 mg, 1.4 mmol), in one portion, and glacial acetic acid (0.18 mL, 3 mmol). The mixture was heated in the microwave reactor at 80° C. for 1 hour. After this time the mixture was stirred with dilute aqueous hydrochloric acid (2M, 7 mL) for 15 minutes and the two phases were separated. The aqueous phase was basified to pH 9 with solid potassium hydroxide and was extracted with dichloromethane (2×20 mL). The extracts were washed with brine (20 mL), dried (MgSO4) and concentrated under reduced pressure to give an orange oil which was purified by flash chromatography (silica, ethyl acetate/methanol) to give 6-chloro-N-[(1S)-1-(3-{[1-(3-methylphenyl)ethyl]amino}phenyl)ethyl]pyrazin-2-amine (52 mg, 14%) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029386B2
出典データセットuspto-grants-2015_05
ORD IDord-0be33a69c4534afe957e0d5d4eb4bbc3
出典メモuspto-grants-2015_05