1-Methyl-4-piperidone → HCID 14973214, compound

HRID 973960Notes

Reaction equation

HRID 973960 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.[NH:9]1[C:17]2[C:12](=[CH:13][C:14]([C:18]([O:20][CH3:21])=[O:19])=[CH:15][CH:16]=2)[CH:11]=[CH:10]1>>[CH3:1][N:2]1[CH2:7][CH:6]=[C:5]([C:11]2[C:12]3[C:17](=[CH:16][CH:15]=[C:14]([C:18]([O:20][CH3:21])=[O:19])[CH:13]=3)[NH:9][CH:10]=2)[CH2:4][CH2:3]1

Participants

3

Procedure

Following the method of Example 1, N-methyl-4-piperidone (-0.68 g) and methyl 1H-indole-5-carboxylate (0.5 g) gave the title compound as microcrystals (0.18 g), m.p. 202°-204° following recrystallisation from ethyl acetate.

Sources & evidence

ORD record
ord-e1a949ec329e4295ab72a83ce0aba3a8
Source dataset
uspto-grants-1991_11
Patent number
US05066660

Reaction notes

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