4-Methoxybenzoic Acid → HCID 66763070, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:33]=[CH:32][C:6]([C:7]([N:9](C)[C:10]2[CH:11]=[C:12]([CH:28]=[CH:29][CH:30]=2)[CH2:13][NH:14][C:15]2[C:24]3[C:19](=[C:20]([C:25]([NH2:27])=[O:26])[CH:21]=[CH:22][CH:23]=3)[N:18]=[CH:17][N:16]=2)=[O:8])=[CH:5][CH:4]=1.NC1C([F:43])=C(C=CC=1)C#N.COC1C=CC(C(O)=O)=CC=1>>[F:43][C:11]1[C:10]([NH:9][C:7](=[O:8])[C:6]2[CH:32]=[CH:33][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[CH:30][CH:29]=[CH:28][C:12]=1[CH2:13][NH:14][C:15]1[C:24]2[C:19](=[C:20]([C:25]([NH2:27])=[O:26])[CH:21]=[CH:22][CH:23]=2)[N:18]=[CH:17][N:16]=1Participants
4
Procedure
The title compound was prepared according to example 4-{3-[(4-Methoxy-benzoyl)-methyl-amino]-benzylamino}-quinazoline-8-carboxylic acid amide, starting from 3-Amino-2-fluoro-benzonitrile and 4-Methoxy-benzoic acid:
Sources & evidence
- ORD record
- ord-075fda0194164b08a1df59b450438a02
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040560B2
Reaction notes
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