Hydrazine → HCID 178491797, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([C:9]([C:11]2[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:12]=2[O:18][CH3:19])=O)=[CH:4][N:3]=1.[NH2:20][NH2:21]>C1COCC1>[Cl:1][C:2]1[N:7]=[C:6]2[NH:20][N:21]=[C:9]([C:11]3[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:12]=3[O:18][CH3:19])[C:5]2=[CH:4][N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of (2,4-dichloro-pyrimidin-5-yl)-(5-fluoro-2-methoxy-phenyl)-methanone (602 mg, 2 mmol) in THF (8 m), hydrazine (Aldrich, 98%, 64 mg, 2 mmol) was added and the mixture was stirred for 20 minutes followed by a second portion of hydrazine (0.1 mL). The reaction finished in 5 minutes. The solvent was removed and the solid was washed with water/acetonitrile (3:1) to give a yellow solid. 456 mg, 82%. MS (M+H)+, 278.
Workup
- waitThe reaction finished in 5 minutes
- customThe solvent was removed
- washthe solid was washed with water/acetonitrile (3:1)
- customto give a yellow solid
Sources & evidence
- ORD record
- ord-cf00f8f22bcf4727a9704597d8d2e13c
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405220B2
Reaction notes
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