HCID 14704562, compound → HCID 25263717, compound

HRID 1516556Notes

Reaction equation

HRID 1516556 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].[OH:21][CH:22]1[CH:31]([OH:32])[C:30]2[C:25](=[CH:26][CH:27]=[C:28]([C:33](O)=[O:34])[CH:29]=2)[O:24][C:23]1([CH3:37])[CH3:36]>>[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[NH:20][C:33]([C:28]1[CH:29]=[C:30]2[C:25](=[CH:26][CH:27]=1)[O:24][C:23]([CH3:37])([CH3:36])[CH:22]([OH:21])[CH:31]2[OH:32])=[O:34]

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 3,4-Dihydroxy-2,2-dimethyl-chroman-6-carboxylic acid. MS: 494.6 (M+H).

Sources & evidence

ORD record
ord-641d24bb7f8d48dfb83d3a801f5e0a01
Source dataset
uspto-grants-2012_07
Patent number
US08227504B2

Reaction notes

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