62718-28-9

基本信息
1-甲基哌啶-4-羧酰胺
1-甲基異3-哌啶甲酰胺
1-METHYLPIPERIDINE-4-CARBOXAMIDE
N-METHYLPIPERIDINE-4-CARBOXAMIDE
1-Methyl-4-PiperidinecarboxaMide
4-Piperidinecarboxamide, 1-methyl-
4-Piperidinecarboxamide,1-methyl-(9CI)
制備方法

39546-32-2

50-00-0

62718-28-9
將哌啶-4-甲酰胺(10 g,78 mmol)溶于蒸餾水(100 mL)中,加入37%甲醛水溶液(7.6 mL,相當于2.81 g HCHO,93.6 mmol)。在氬氣保護下,加入濕的10% Pd/C催化劑(8刮刀勺),并將混合物在25℃和50 psi氫氣壓力下氫化43小時。反應完成后,通過硅藻土過濾除去催化劑,催化劑用水和甲醇洗滌。合并濾液,蒸發(fā)至干。殘余物通過硅膠柱色譜(60×5 cm)純化,使用8%-10%-20%(10%濃氨水的甲醇溶液)-二氯甲烷作為洗脫液,得到1-甲基哌啶-4-羧酰胺(7.15 g,產(chǎn)率64%)。產(chǎn)物表征數(shù)據(jù)如下:FABMS:m/z 143.1(MH+);HRFABMS:m/z 143.1184(MH+),計算值C7H15N2O:m/z 143.1184;1H NMR(d6-DMSO)δ 1.50-1.57(4H,m,CH2),1.76-1.94(4H,m,CH2),2.10(3H,s,-NCH3),2.72(1H,m,CH),6.68-7.18(2H,m,CONH2);13C NMR(d6-DMSO)δ 41.2(CH3),28.5, 28.5, 54.9, 54.9(CH2),46.2(CH),176.7(C)。
參考文獻:
[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 7, p. 1116 - 1119
[2] Patent: WO2004/22561, 2004, A1. Location in patent: Page 110
[3] Journal of Medicinal Chemistry, 2005, vol. 48, # 24, p. 7520 - 7534
[4] Helvetica Chimica Acta, 1954, vol. 37, p. 1672,1676