Aniline → HCID 58168022, compound

HRID 1029246Notes

Reaction equation

HRID 1029246 reaction equation
C([NH:8][C:9]([C:11]1[N:12]([CH3:32])[CH:13]=[C:14]([NH:16][C:17]2[CH:26]=[CH:25][N:24]=[C:23]3[C:18]=2[C:19]2[CH:31]=[CH:30][CH:29]=[CH:28][C:20]=2[C:21](=[O:27])[NH:22]3)[CH:15]=1)=[O:10])C1C=CC=CC=1.N[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>>[CH3:32][N:12]1[CH:13]=[C:14]([NH:16][C:17]2[CH:26]=[CH:25][N:24]=[C:23]3[C:18]=2[C:19]2[CH:31]=[CH:30][CH:29]=[CH:28][C:20]=2[C:21](=[O:27])[NH:22]3)[CH:15]=[C:11]1[C:9]([NH:8][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)=[O:10]

Participants

3

Reactant 2

HCID 6115AnilineHCID 58167955HCID 58167955, compound

Product 1

HCID 58168022HCID 58168022, compound

Procedure

The title compound was synthesized according to the procedure described for the preparation of Example 300 using the carboxylic acid intermediate from example 310 and aniline to provide 312. LC-MS (M+H=410, obsd.=410).

Workup

  1. customThe title compound was synthesized

Sources & evidence

ORD record
ord-a5497c3a2bc64418b416aaf3e9747382
Source dataset
uspto-grants-2014_05
Patent number
US08735584B2

Reaction notes

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