2-(2-t-Butoxycarbonylaminopyridin-4-yl)-3-dimethylamino-1-(3-trifluoromethylphenyl)-2-propen-1-one → HCID 178452639, compound
Reaction equation
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:14]=[C:13]([C:15](=[CH:28][N:29](C)C)[C:16]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([C:24]([F:27])([F:26])[F:25])[CH:19]=2)=O)[CH:12]=[CH:11][N:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(OC([NH:39]C1C=C(C(=CN(C)C)C(C2C=CC(F)=CC=2)=O)C=CN=1)=O)(C)(C)C>>[C:1]([O:5][C:6]([NH:8][C:9]1[CH:14]=[C:13]([C:15]2[C:16]([C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([C:24]([F:27])([F:26])[F:25])[CH:19]=3)=[N:39][NH:29][CH:28]=2)[CH:12]=[CH:11][N:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The reaction was carried out in the same manner as in Example 2-2) except for using 8.71 g (20.0 mmol) of 2-(2-t-butoxycarbonylaminopyridin-4-yl)-3-dimethylamino-1-(3-trifluoromethylphenyl)-2-propen-1-one obtained in Example 25-1) in place of 2-(2-t-butoxycarbonylaminopyridin-4-yl)-3-dimethylamino-1-(4-fluorophenyl)-2-propen-1-one to obtain 7.76 g of the title compound as a white powder. (Yield: 96%)
Sources & evidence
- ORD record
- ord-7809a29e016e4bb5a2bad6e59c6c26a1
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07294625B2
Reaction notes
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