6-(3-Cyano-thiophen-2-yl)-2,2-dimethyl-[1,3]dioxin-4-one → {3-[3-(3-Cyano-thiophen-2-yl)-3-oxo-propionylamino]-4'-fluoro-biphenyl-4-yl}-carbamic acid tert.-butyl ester
Reaction equation
[C:1]([O:5][C:6](=[O:22])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)=[CH:10][C:9]=1[NH2:21])([CH3:4])([CH3:3])[CH3:2].[C:23]([C:25]1[CH:29]=[CH:28][S:27][C:26]=1[C:30]1[O:35]C(C)(C)[O:33][C:32](=O)[CH:31]=1)#[N:24]>>[C:1]([O:5][C:6](=[O:22])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:15]=[CH:16][C:17]([F:20])=[CH:18][CH:19]=2)=[CH:10][C:9]=1[NH:21][C:32](=[O:33])[CH2:31][C:30]([C:26]1[S:27][CH:28]=[CH:29][C:25]=1[C:23]#[N:24])=[O:35])([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
Prepared from (3-amino-4′-fluoro-biphenyl-4-yl)-carbamic acid tert.-butyl ester (Example G39) (302 mg, 1.0 mmol) and 6-(3-cyano-thiophen-2-yl)-2,2-dimethyl-[1,3]dioxin-4-one (Example J3) (250 mg, 1.06 mmol) according to the general procedure K. Obtained as a light yellow solid (251 mg).
Sources & evidence
- ORD record
- ord-53ad8f0704134077b03933f319057dd2
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06960578B2
Reaction notes
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