HCID 67135286, compound → HCID 67135682, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([C:17]([F:20])([F:19])[F:18])=[C:7]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])[CH:8]=1)#[N:2]>[Ni].C1COCC1>[NH2:2][CH2:1][C:3]1[CH:4]=[CH:5][C:6]([C:17]([F:18])([F:19])[F:20])=[C:7]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:13])[CH3:14])[CH:8]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The sub-title compound was prepared in accordance with the procedure in Example 59, step (g) using tert-butyl N-[5-cyano-2-(trifluoromethyl)phenyl]-carbamate (8.5 g; 29.7 mmol), Ra—Ni (174 mg; 2.97 mmol), H2 (5 atm) and THF (60 mL). Yield: 8 g (93%).
Sources & evidence
- ORD record
- ord-b79659446da2465ca94ce2ef259d9ae3
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921405B2
Reaction notes
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