HCID 4052667, compound → HCID 19738031, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[CH:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[C:9]#[N:10])=[CH:4][CH:3]=1.[BH4-].[Na+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[C:9]#[N:10])=[CH:6][CH:7]=1Participants
3
Procedure
This intermediate (64 g.) was prepared using the procedure described in Example 12b except using 80 g. (0.3 mole) of 2-(4-chlorophenyl)-3-(3-pyridyl)acrylonitrile, and 14 g. (0.36 mole) of sodium borohydride.
Workup
- customThis intermediate (64 g.) was prepared
Sources & evidence
- ORD record
- ord-5160fbaebb17448aa4fa16ce8eaf9a31
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05240925
Reaction notes
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