Isopropanol → HCID 23093005, compound
Reaction equation
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([OH:10])[CH:7]=[C:6](OCOC)[CH:5]=1.Br[C:17]1[CH:18]=[CH:19][C:20]([S:23]([CH3:26])(=[O:25])=[O:24])=[N:21][CH:22]=1.[NH2:27][C:28]1[CH:32]=[CH:31][N:30]([CH3:33])[N:29]=1.[OH:34][CH:35]([CH3:37])[CH3:36]>>[CH:35]([O:34][C:6]1[CH:7]=[C:8]([O:10][C:17]2[CH:22]=[N:21][C:20]([S:23]([CH3:26])(=[O:25])=[O:24])=[CH:19][CH:18]=2)[CH:9]=[C:4]([CH:5]=1)[C:3]([NH:27][C:28]1[CH:32]=[CH:31][N:30]([CH3:33])[N:29]=1)=[O:2])([CH3:37])[CH3:36]Participants
5
Procedure
The compound of Production Example 130 was obtained as a white amorphous substance using 5-hydroxy-3-methoxymethoxybenzoic acid methyl ester, 5-bromo-2-methanesulfonylpyridine, 2-hydroxypropane 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 130 was obtained as a white amorphous substance
Sources & evidence
- ORD record
- ord-c771d5d21c304033a481ce5ddd951cc2
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07432287B2
Reaction notes
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