3-Chloroisoquinoline-4-carbaldehyde → 1-(3-Chloro-isoquinolin-4-yl)-4-phenyl-butan-1-ol
Reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[C:10]([C:11]=1[CH:12]=[O:13])=[CH:9][CH:8]=[CH:7][CH:6]=2.[C:14]1([CH2:20][CH2:21][CH2:22][Mg]Br)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[C:10]([C:11]=1[CH:12]([OH:13])[CH2:22][CH2:21][CH2:20][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2Participants
3
Procedure
Prepared according to the procedure described in Example 5, Step 1, using the following starting materials: 3-chloro-isoquinoline-4-carbaldehyde and 3-phenyl-propyl magnesium bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-97dbd75c09e54d82aa6859fb0bbf4602
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09272990B2
Reaction notes
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