1-methylpiperidine-3-carboxylic Acid → HCID 72399616, compound

HRID 1242584Notes

Reaction equation

HRID 1242584 reaction equation
[C:1]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:6]=[CH:5][C:4]([C:7]([N:9]2[CH2:13][C:12](=[N:14][O:15][CH3:16])[CH2:11][C@H:10]2[C:17](=[N:19][OH:20])[NH2:18])=[O:8])=[CH:3][CH:2]=1.[CH3:27][N:28]1[CH2:33][CH2:32][CH2:31][CH:30]([C:34](O)=O)[CH2:29]1>>[CH3:16][O:15][N:14]=[C:12]1[CH2:11][CH:10]([C:17]2[N:18]=[C:34]([CH:30]3[CH2:31][CH2:32][CH2:33][N:28]([CH3:27])[CH2:29]3)[O:20][N:19]=2)[N:9]([C:7]([C:4]2[CH:3]=[CH:2][C:1]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:6][CH:5]=2)=[O:8])[CH2:13]1

Participants

3

Procedure

Following the general method as outlined in Example 15, starting from (2S,4EZ)-1-([1,1′-biphenyl]-4-ylcarbonyl)-N′-hydroxy-4-(methoxyimino)-2-pyrrolidinecarboximidamide (Intermediate 8) and 1-methyl-3-piperidinecarboxylic acid, the title compound was obtained in 72% yield (99.2% purity by HPLC).

Sources & evidence

ORD record
ord-9c8cb47f32424607a3044ac36e1e47cb
Source dataset
uspto-grants-2006_10
Patent number
US07115639B2

Reaction notes

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