Dimethylformamide diethylacetal → 3-Dimethylamino-1-(2-chloro4-pyridyl)-2-propen-1-one
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([Cl:10])[CH:5]=1)(=[O:3])[CH3:2].C(O[CH:14](OCC)[N:15]([CH3:17])[CH3:16])C>>[CH3:14][N:15]([CH3:17])[CH:16]=[CH:2][C:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([Cl:10])[CH:5]=1)=[O:3]Participants
3
Procedure
16.2 g (104.2 mmol) of 4-acetyl-2-chloro-pyridine are stirred for 1 h at 110° with 116 ml of dimethylformamide diethylacetal. After cooling to 0°, filtering and drying at 60° under HV, 3-dimethylamino-1-(2-chloro-4-pyridyl)-2-propen-1-one is obtained; 1H-NMR (dimethyl sulfoxide): 2.98 (3H,s), 3.2 (3H,s), 5.9 (1H,d), 7.8 (3H.m), 8.5
Workup
- temperatureAfter cooling to 0°
- filtrationfiltering
- customdrying at 60° under HV
Sources & evidence
- ORD record
- ord-3df333092fae4c72812d3a4dc3f1bbf4
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05612340
Reaction notes
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