Hydrazine hydrate (1:1) → HCID 178480054, compound
Reaction equation
[Cl:1][C:2]1[CH:25]=[C:24]([C:26]2[CH:27]=[N:28][N:29]([CH3:31])[CH:30]=2)[CH:23]=[CH:22][C:3]=1[CH2:4][CH:5]1[CH2:9][CH2:8][N:7]([CH:10]2[CH2:15][CH2:14][C:13](=O)[C:12](=[CH:17][N:18](C)C)[CH2:11]2)[C:6]1=[O:21].O.[NH2:33]N>CO>[Cl:1][C:2]1[CH:25]=[C:24]([C:26]2[CH:27]=[N:28][N:29]([CH3:31])[CH:30]=2)[CH:23]=[CH:22][C:3]=1[CH2:4][CH:5]1[CH2:9][CH2:8][N:7]([CH:10]2[CH2:15][CH2:14][C:13]3[C:12](=[CH:17][NH:18][N:33]=3)[CH2:11]2)[C:6]1=[O:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve 3-[2-Chloro-4-(1-methyl-1H-pyrazol-4-yl)-benzyl]-1-(3-dimethylaminomethylene-4-oxo-cyclohexyl)-pyrrolidin-2-one (Preparation 30) (0.327 g, 0.745 mmol) in methanol (3.0 mL), and hydrazine hydrate (0.038 mL) stir the resulting orange solution for 17 hours at room temperature. Filter the mixture, rinse with cold methanol and vacuum dry to 0.138 g of a solid. MS (m/z): 410 (M+1).
Workup
- filtrationFilter the mixture
- washrinse with cold methanol and vacuum
- dry with materialdry to 0.138 g of a solid
Sources & evidence
- ORD record
- ord-9bbb66d50fcc4326a936b7fe4ff0207c
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07981918B2
Reaction notes
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