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HRID 61463作成日:2026年10月25日

Dimethylformamide → Methyl (2s,3s,5s)-2-[(4-phenyl-3,6-dihydropyridin-1(2h)-yl)carbonyl]-5-[(pyrrolidin-1-ylcarbonyl)oxy]piperidine-3-carboxylate

https://huagongshe.com/reaction/61463

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物DiisopropylethylamineHCID 81531—
反応物1,2,3,6-Tetrahydro-4-phenylpyridineHCID 82553—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物(2s,3s,5s)-3-(Methoxycarbonyl)-5-[(pyrrolidin-1-ylcarbonyl)oxy]piperidine-2-carboxylic acidHCID 67304698—
生成物Methyl (2s,3s,5s)-2-[(4-phenyl-3,6-dihydropyridin-1(2h)-yl)carbonyl]-5-[(pyrrolidin-1-ylcarbonyl)oxy]piperidine-3-carboxylateHCID 67304271—

反応手順

To a mixture of (2S,3S,5S)-3-(methoxycarbonyl)-5-[(pyrrolidin-1-ylcarbonyl)oxy]piperidine-2-carboxylic acid (90.1 mg, 0.000300 mol) and 4-phenyl-1,2,3,6-tetrahydropyridine (64.6 mg, 0.000330 mol) HCl salt, benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (146 mg, 0.000330 mol) in N,N-dimethylformamide (0.44 mL, 0.0057 mol) was added N,N-diisopropylethylamine (0.115 mL, 0.000660 mol) at rt. The mixture was stirred at rt overnight, then quenched with aq. sodium bicarbonate. After separation of the organic layers, the aq. layer was extracted with EtOAc. The combined organic layers were washed with brine, dried, and concentrated to dry. The crude material was used directly in next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440958B2
出典データセットuspto-grants-2016_09
ORD IDord-8f429a7246e44e3396caab35b3332f8a
出典メモuspto-grants-2016_09