1,3-Difluoro-2-propanol → HCID 23093082, compound
Reaction equation
CO[C:3](=[O:15])[C:4]1[CH:9]=[C:8]([OH:10])[CH:7]=[C:6](OCOC)[CH:5]=1.Cl.Cl[C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1.[F:24][CH2:25][CH:26]([OH:29])[CH2:27][F:28].[NH2:30][C:31]1[CH:35]=[CH:34][N:33]([CH3:36])[N:32]=1>>[F:24][CH2:25][CH:26]([CH2:27][F:28])[O:29][C:6]1[CH:7]=[C:8]([O:10][C:18]2[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=2)[CH:9]=[C:4]([CH:5]=1)[C:3]([NH:30][C:31]1[CH:35]=[CH:34][N:33]([CH3:36])[N:32]=1)=[O:15]Participants
5
Procedure
The compound of Production Example 164 was obtained as a white amorphous substance using 5-hydroxy-3-methoxymethoxybenzoic acid methyl ester, 4-chloropyridine hydrochloride, 1,3-difluoro-2-propanol and 3-amino-1-methyl-1H-pyrazole, by the same method as in Production Example 117, a corresponding method, or a combination thereof with an ordinary method.
Workup
- customThe compound of Production Example 164 was obtained as a white amorphous substance
Sources & evidence
- ORD record
- ord-f4749c5936734638a88b95f9a9ff7c3d
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07432287B2
Reaction notes
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