4-(3-Fluorophenyl)butan-2-one → 4-[N'-(1-methyl-3-(3-fluorophenyl)-propylidene)-hydrazino]-1H-pyridin-2-one
Reaction equation
[NH:1]([C:3]1[CH:8]=[CH:7][NH:6][C:5](=[O:9])[CH:4]=1)[NH2:2].[F:10][C:11]1[CH:12]=[C:13]([CH:19]=[CH:20][CH:21]=1)[CH2:14][CH2:15][C:16](=O)[CH3:17]>>[CH3:17][C:16](=[N:2][NH:1][C:3]1[CH:8]=[CH:7][NH:6][C:5](=[O:9])[CH:4]=1)[CH2:15][CH2:14][C:13]1[CH:19]=[CH:20][CH:21]=[C:11]([F:10])[CH:12]=1Participants
3
Procedure
In accordance with the same procedures as in Step 2 of Preparation 1, except for using 4-hydrazino-1H-pyridin-2-one (5.39 g, 43.1 mmol) prepared in Step 1 of Preparation 1 and 3-fluorobenzylacetone (9.82 ml, 65.1 mmol), the titled compound was obtained as a white solid. (Yield: 63.4%) The product was used in the subsequent reaction without further purification.
Workup
- customIn accordance with the same procedures as in Step 2 of Preparation 1
Sources & evidence
- ORD record
- ord-a84cd9789cab48c49994923261d5e840
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513277B2
Reaction notes
Loading…