3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic Acid → HCID 86661861, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[N:9]([CH3:26])[C:10](=[O:25])[C:11]([CH3:24])([CH3:23])[C@:12]([C:15]2[CH:20]=[C:19]([NH2:21])[CH:18]=[CH:17][C:16]=2[F:22])([CH3:14])[N:13]=1)(C)(C)C.[F:28][C:29]([F:40])([F:39])[C:30]([OH:38])([C:34]([F:37])([F:36])[F:35])[C:31](O)=[O:32]>>[NH2:7][C:8]1[N:9]([CH3:26])[C:10](=[O:25])[C:11]([CH3:24])([CH3:23])[C@:12]([C:15]2[CH:20]=[C:19]([NH:21][C:31](=[O:32])[C:30]([OH:38])([C:29]([F:28])([F:39])[F:40])[C:34]([F:37])([F:36])[F:35])[CH:18]=[CH:17][C:16]=2[F:22])([CH3:14])[N:13]=1Participants
3
Procedure
The coupling of [(S)-4-(5-amino-2-fluoro-phenyl)-1,4,5,5-tetramethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester (intermediate F) and 3,3,3-trifluoro-2-hydroxy-2-trifluoromethyl-propionic acid followed by deprotection of the intermediate yielded the title compound as a colorless amorphous solid. MS (ESI): m/z=473.3 [M+H]+.
Sources & evidence
- ORD record
- ord-2a7ca1505d254c339e868ad081678164
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815881B2
Reaction notes
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