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HRID 15896作成日:2026年10月26日

tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate → 1,1-Dimethylethyl 2-{[(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)amino]methyl}-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/15896

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl (2S)-2-formylpyrrolidine-1-carboxylateHCID 2734674—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}anilineHCID 49852105—
溶媒MethanolHCID 887—
生成物1,1-Dimethylethyl 2-{[(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)amino]methyl}-1-pyrrolidinecarboxylateHCID 7654098540%

反応手順

3-{2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline (D6, 115 mg) and N-(tert-butoxycarbonyl)-L-prolinal (1.2 equiv., 79 mg) were stirred in methanol (2 mL) until the mixture became a clear solution. Then, sodium triacetoxyborohydride (1.2 eq., 85 mg) was added. After 24 h the reaction mixture was loaded onto an ion-exchange cartridge (SCX-2) and eluted with methanol followed by ammonia/methanol (1M). The combined basic fractions were concentrated in vacuo and purified by column chromatography (SPE cartridge, silica) using DCM-methanol (95:5) as eluent to afford the title compound (70 mg, 40% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732600B2
出典データセットuspto-grants-2010_06
ORD IDord-b0acdd14acef4026b9ce9afd20bda0b3
出典メモuspto-grants-2010_06