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HRID 527475作成日:2026年10月25日

Acetic Acid → rac-[(3R,4S)-3-(3,4-Dichloro-phenyl)-4-isopropylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanone

https://huagongshe.com/reaction/527475

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AcetoneHCID 180—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物rac-(3S,4R)-[3-Amino-4-(3,4-dichloro-phenyl)-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 67238593—
溶媒DichloromethaneHCID 6344—
生成物rac-[(3R,4S)-3-(3,4-Dichloro-phenyl)-4-isopropylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 6723926172.7%

反応手順

To a solution of rac-(3S,4R)-[3-Amino-4-(3,4-dichloro-phenyl)-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanone (120 mg, 0.28 mmol) in dichloromethane (1 mL) were added acetone (21 uL, 0.28 mmol) and sodiumtriacetoxy-borohydride (72 mg, 0.34 mmol) and acetic acid (16 uL, 0.28 mmol) and the reaction mixture was stirred at ambient temperature for 3 h. It was diluted with dichloromethane and washed with aqueous sodiumhydrogenecarbonate (1M). The organic layer was dried over sodium sulfate and concentrated affording the title compound (95 mg, 72%) as a light yellow foam. MS m/e: 466.3 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346786B2
出典データセットuspto-grants-2016_05
ORD IDord-b1f5d3f418794183afe571eaf96ebb02
出典メモuspto-grants-2016_05