Chloroform → HCID 54414068, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([F:12])([F:11])[F:10])=[CH:5][C:4]=1[NH:13][C:14](Cl)=[O:15].[NH2:17][C:18]1[C:27]2[CH2:26][CH2:25][CH2:24][CH2:23][C:22]=2[CH:21]=[CH:20][CH:19]=1.C(N(CC)CC)C.C(Cl)(Cl)Cl>O>[C:18]1([NH:17][C:14]([NH:13][C:4]2[CH:5]=[C:6]([C:9]([F:12])([F:11])[F:10])[CH:7]=[CH:8][C:3]=2[O:2][CH3:1])=[O:15])[C:27]2[CH2:26][CH2:25][CH2:24][CH2:23][C:22]=2[CH:21]=[CH:20][CH:19]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
2-methoxy-5-(trifluoromethyl)phenyl carbamoylchloride (0.81 g, 3.2 mmol), 1-amino-5,6,7,8-tetrahydronaphtalene (445 μl, 3.2 mmol) and triethylamine (446 μl, 3.2 mmol) were added to chloroform (20 ml) and the resulting mixture was stirred at RT overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The solvent was evaporated in vacuuo and the residue recrystallized from toluene (20 ml). 0.45 g of the title compound was isolated.
Workup
- extractionextracted with ethyl acetate
- customThe solvent was evaporated in vacuuo
- customthe residue recrystallized from toluene (20 ml)
Sources & evidence
- ORD record
- ord-2428f200bbd14f1da9e51da695eb33bb
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05696138
Reaction notes
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