Cyclopropanecarboxylic acid → HCID 66558859, compound
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.[CH:18]1([C:21](O)=[O:22])[CH2:20][CH2:19]1>>[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:21]([CH:18]3[CH2:20][CH2:19]3)=[O:22])[CH:3]=[CH:4][C:5]=2[F:17])([CH3:16])[N:9]=1Participants
3
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 cyclopropanecarboxylic acid following procedure I yielded the title compound as a white foam. MS (ISP): m/z=310.2 [M+H]+.
Sources & evidence
- ORD record
- ord-9f5a8bc2415c4e84a04c0ab2989fb40d
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09115098B2
Reaction notes
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