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HRID 417522作成日:2026年10月26日

4,4'-Diazenediyldianiline → N-Boc-pyrrolidine

https://huagongshe.com/reaction/417522

反応式

関与物質

役割名称HCID仕込み量
反応物4,4'-DiazenediyldianilineHCID 10855—
反応物1(2H)-Quinolinecarboxylic acid, ethyl esterHCID 27813—
反応物1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
溶媒DichloromethaneHCID 6344—
生成物N-Boc-pyrrolidineHCID 643455166.6%

反応手順

4-(4-aminophenylazo)-phenylamine (3.02 g) and pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (7.00 g) were dissolved in DCM (90 mL), and 1-ethoxycarbonyl-1,2-dihydroquinoline (8.45 g) was added. The reaction mixture was stirred at ambient temperature for 19 hours and evaporated under vacuum. Oil was dissolved in ethyl acetate, forming a precipitate, which was collected by vacuum filtration and dried under vacuum, giving 2-(4-{4-[(1-carboxylic acid tert-butyl ester-pyrrolidine-2-carbonyl)-amino]-phenylazo}-phenylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (9.28 g) as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088368B2
出典データセットuspto-grants-2012_01
ORD IDord-0f87618dd8434b21a9cc9b11191b8452
出典メモuspto-grants-2012_01