Sodium hydride → HCID 22633017, compound
Reaction equation
[CH2:1]([O:8][NH:9][C:10]([C:12]1[C:13](Cl)=[N:14][C:15]([Cl:19])=[C:16]([F:18])[CH:17]=1)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[CH2:23]([N:30]=[C:31]=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>CC(N(C)C)=O>[CH2:23]([N:30]1[C:13]2[N:14]=[C:15]([Cl:19])[C:16]([F:18])=[CH:17][C:12]=2[C:10](=[O:11])[N:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:31]1=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Using the General Method 5, the reaction of N-benzyloxy-2,6-dichloro-5-fluoro-3-pyridinecarboxamide (Example M-2, 2.00 g, 6.34 mmol) and 60% NaH in oil (300 mg, 7.52 mmol) with benzyl isocyanate (1.17 mL, 9.51 mmol) in DMA afforded crude product. Recrystallization from chloroform provided 2.15 g of the title compound as a solid, mp 209-210° C.
Workup
- customafforded crude product
- customRecrystallization from chloroform
Sources & evidence
- ORD record
- ord-1d5c176e7dc74d25ba26725541e62cb3
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331538B1
Reaction notes
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