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HRID 2371162作成日:2026年10月25日

Tert-butyl 3-oxopyrrolidine-1-carboxylate → Tert-butyl 3-(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2371162

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 3-(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)pyrrolidine-1-carboxylateHCID 5765674088%

反応手順

N-(3,4-dichlorophenyl)piperazine-1-carboxamide (0.548 g, 2 mmols) and 1-N-BOC-3-pyrrolidinone (370 mg, 2 mmols) were stirred at room temperature in dichloromethane (20 ml) for approximately 15 minutes. Added to this mixture was sodium triacetoxyborohydride (1.06 g, 5 mmols) and the reaction stirred overnight at room temperature. Saturated sodium bicarbonate solution (5 ml) was added and the mixture stirred for 1 hour then poured onto a hydromatrix column and the product eluted with dichloromethane (100 ml). The crude product was subjected to chromatography on silica gel (50 g) using a gradient of 100% dichloromethane through to 10% methanolic ammonia in dichloromethane to give the title compound as a white solid (780 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08710224B2
出典データセットuspto-grants-2014_04
ORD IDord-b6664c3020db4a2e8ff25157af194f1e
出典メモuspto-grants-2014_04