Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([C@:8]2([CH3:16])[C@@H:13]([F:14])[CH2:12][O:11][C:10]([NH2:15])=[N:9]2)[CH:7]=1.[CH3:18][C:19]1[O:20][C:21]([CH3:27])=[CH:22][C:23]=1[C:24](O)=[O:25]>>[NH2:15][C:10]1[O:11][CH2:12][C@H:13]([F:14])[C@:8]([C:6]2[CH:7]=[C:2]([NH:1][C:24]([C:23]3[CH:22]=[C:21]([CH3:27])[O:20][C:19]=3[CH3:18])=[O:25])[CH:3]=[CH:4][C:5]=2[F:17])([CH3:16])[N:9]=1Participants
3
Reactant 2
Product 1
Procedure
The condensation of (4R,5R)-4-(5-amino-2-fluoro-phenyl)-5-fluoro-4-methyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (intermediate A8.2) and 2,5-dimethyl-furan-3-carboxylic acid (CAS 636-44-2) following procedure I yielded the title compound as a white solid. MS (ISP): m/z=364.3 [M+H]+.
Sources & evidence
- ORD record
- ord-9c1dddec40c04694a5db672411002dd5
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754075B2
Linked notes
Loading…