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HRID 459724作成日:2026年10月26日

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/459724

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物4-PiperidinecarboxamideHCID 3772—
触媒PalladiumHCID 23938—
溶媒WaterHCID 962—
生成物1-Methylpiperidine-4-carboxamideHCID 33901164.5%

反応手順

Isonipecotamide (10 g, 78.0 mmoles) was dissolved in distilled water (100 mL) and 37% aqueous formaldehyde (7.6 mL, equivalent to 2.81 g HCHO, 93.6 mmoles) was added. Wet 10% Pd—C (8 spoon spatulas) was added under argon and the mixture was hydrogenated at 25° C. and 50 psi for 43 h. The catalyst was filtered off through Celite and the latter was washed with water and methanol. The combined filtrates were evaporated to dryness and the residue was chromatographed on a silica gel column (60×5 cm) using 8%–10%–20% (10% conc. ammonium hydroxide in methanol)-dichloromethane as the eluant to give 1-methylisonipecotamide (7.15 g, 64%): FABMS: m/z 143.1 (MH+); HRFABMS: m/z 143.1184 (MH+). Calcd. for C7H15N2O: m/z 143.1184; δH (d6-DMSO) 1.50/1.57 (4H, m, CH2), 1.76/1.94 (4H, m, CH2), 2.10 (3H, s, —NCH3), 2.72 (1H, m, CH) and 6.68/7.18 ppm (2H, m, CONH2); δC (d6-DMSO)CH3: 41.2; CH2: 28.5, 28.5, 54.9, 54.9; CH: 46.2; C: 176.7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196078B2
出典データセットuspto-grants-2007_03
ORD IDord-967c34a506014927805b854263b564a2
出典メモuspto-grants-2007_03