HCID 21806936, compound → HCID 25265670, compound

HRID 1516547Notes

Reaction equation

HRID 1516547 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N:8]2[CH2:12][CH2:11][CH:10]([CH2:13][N:14]3[CH2:18][CH2:17][CH2:16][CH:15]3[CH3:19])[CH2:9]2)[CH:5]=[CH:4][C:3]=1[NH2:20].[CH2:21]([O:28][CH2:29][C:30]1[CH:38]=[CH:37][C:33]([C:34](O)=[O:35])=[CH:32][N:31]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[CH2:21]([O:28][CH2:29][C:30]1[CH:38]=[CH:37][C:33]([C:34]([NH:20][C:3]2[CH:4]=[CH:5][C:6]([N:8]3[CH2:12][CH2:11][CH:10]([CH2:13][N:14]4[CH2:18][CH2:17][CH2:16][CH:15]4[CH3:19])[CH2:9]3)=[CH:7][C:2]=2[CH3:1])=[O:35])=[CH:32][N:31]=1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

3

Procedure

The title compound was prepared in a manner substantially the same as Example 1 by coupling 2-methyl-4-[3-(2-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-phenylamine with 6-benzyloxymethyl-nicotinic acid. MS: 499.3 (M+H).

Sources & evidence

ORD record
ord-99510cda7a914dbd8657dec3cd3a3d39
Source dataset
uspto-grants-2012_07
Patent number
US08227504B2

Reaction notes

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