Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:18])=[C:6]([C@:8]2([CH3:17])[C@:13]([F:15])([CH3:14])[CH2:12][O:11][C:10]([NH2:16])=[N:9]2)[CH:7]=1.[Cl:19][C:20]1[C:21]([C:29](O)=[O:30])=[N:22][N:23]([CH2:25][CH:26]([F:28])[F:27])[CH:24]=1>>[NH2:16][C:10]1[O:11][CH2:12][C@@:13]([F:15])([CH3:14])[C@:8]([C:6]2[CH:7]=[C:2]([NH:1][C:29]([C:21]3[C:20]([Cl:19])=[CH:24][N:23]([CH2:25][CH:26]([F:28])[F:27])[N:22]=3)=[O:30])[CH:3]=[CH:4][C:5]=2[F:18])([CH3:17])[N:9]=1Participants
3
Reactant 2
Product 1
Procedure
The condensation of (4R,5R)-4-(5-amino-2-fluoro-phenyl)-5-fluoro-4,5-dimethyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (A8.3) and 4-chloro-1-(2,2-difluoro-ethyl)-1H-pyrazole-3-carboxylic acid (CAS 1006486-42-5) following procedure I yielded the title compound as a white solid. MS (ISP): m/z=448.2 [M+H]+.
Sources & evidence
- ORD record
- ord-e0181c15b3f84f0ab7e578579da82510
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754075B2
Linked notes
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