HCID 19799131, compound → HCID 67858434, compound
Reaction equation
[F:1][C:2]1([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[C:10]([C:18](O)=[O:19])[N:9]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH2:3]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>>[F:1][C:2]1([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[C:10]([CH2:18][OH:19])[N:9]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH2:7]1Participants
3
Procedure
1-(1-Fluorophenyl)-3-isoquinolinecarboxylic acid was converted into its ethylester and then reduced using lithium aluminum hydride to obtain 1-(1-fluorophenyl)-3-isoquinolinemethanol. 1.26 g of the obtained 1-(1-fluorophenyl)-3-isoquinolinemethanol was reacted with 930 mg of methyl p-toluenesulfonate in the same manner as in Reference Example 10 to give 1.6 g of the desired compound as a pale orange-colored solid.
Sources & evidence
- ORD record
- ord-47c0c8f901b349f5871fa268116549e3
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05183811
Reaction notes
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