Sodium hydride → HCID 13851473, compound
Reaction equation
[Cl:1][C:2]1[CH:22]=[CH:21][C:5]([CH2:6][N:7]2[CH:11]=[CH:10][CH:9]=[C:8]2[CH:12]([CH:14]2[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]2)[OH:13])=[C:4](F)[CH:3]=1.[H-].[Na+]>>[Cl:1][C:2]1[CH:22]=[CH:21][C:5]2[CH2:6][N:7]3[CH:11]=[CH:10][CH:9]=[C:8]3[CH:12]([CH:14]3[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]3)[O:13][C:4]=2[CH:3]=1Participants
3
Conditions
- Temperature
- 80 °C
Procedure
A mixture of [1-(4-chloro-2-fluorobenzyl)-2-pyrryl][(1-methyl)piperidin-4-yl]methanol (0.65 g, 0.002 mole) and sodium hydride (50% in oil, 0.12 g, 0.0023 mole, washed once with hexane) in 25 ml 20% DMF/benzene was heated at 80° C. for seven hours.
Workup
- washwashed once with hexane) in 25 ml 20% DMF/benzene
Sources & evidence
- ORD record
- ord-71b6b4d12b92480091f875198a4d1d7f
- Source dataset
- uspto-grants-1987_07
- Patent number
- US04681879
Reaction notes
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