Dimethylamine → N-{4-[(3-bromophenyl)amino]quinazoline-6-yl}4-(dimethylamino)-2-butenamide
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH2:19])[CH:17]=3)[N:12]=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1.Br/C(=C\C)/C(O)=O.CNC.IC1C=C(NC2C3C(=CC=C(N[C:49](=[O:56])[CH:50]=[CH:51][CH2:52][N:53]([CH3:55])[CH3:54])C=3)N=CN=2)C=CC=1>>[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH:19][C:49](=[O:56])[CH:50]=[CH:51][CH2:52][N:53]([CH3:55])[CH3:54])[CH:17]=3)[N:12]=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1Participants
5
Reactant 4
Product 1
Procedure
4-[(3-bromophenyl)amino]-6-aminoquinazoline is reacted with bromocrotonic acid and dimethylamine, as is described hereinabove in Compound 5, to give N-{4-[(3-bromophenyl)amino]quinazoline-6-yl}4-(dimethylamino)-2-butenamide.
Sources & evidence
- ORD record
- ord-3894a2dacea5405f82545427bd925ca1
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07172749B2
Reaction notes
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