Aniline → HCID 178419090, compound
Reaction equation
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][C:5](=[O:11])[NH:6]2.N1C2C(=CC=CC=2)C[C:13]1=O.[N:22]1([CH2:28][CH2:29][CH2:30][NH:31][C:32]2[CH:37]=[CH:36][C:35]([NH2:38])=[CH:34][CH:33]=2)[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1.NC1C=CC=CC=1>>[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=[CH:13][NH:38][C:35]1[CH:36]=[CH:37][C:32]([NH:31][CH2:30][CH2:29][CH2:28][N:22]3[CH2:27][CH2:26][O:25][CH2:24][CH2:23]3)=[CH:33][CH:34]=1)[C:5](=[O:11])[NH:6]2Participants
5
Procedure
The named compound is prepared by substituting 4-methyl-1,3-dihydro-indol-2-one for the 1,3-dihydro-indol-2-one and N-(3-morpholin-4-yl-propyl)-benzene-1,4-diamine (used for the preparation of Example 290) for aniline in the reaction of Example 1.
Workup
- customThe named compound is prepared
- customin the reaction of Example 1
Sources & evidence
- ORD record
- ord-5e9e9595f9b24f91af653c3b48e4f759
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07098236B2
Reaction notes
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