Sodium Bicarbonate → HCID 10131458, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[CH:9][C:8]([C:14]#[N:15])=[C:7]2[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=1)([O-])=O.C(=O)(O)[O-].[Na+]>C(O)C>[NH2:1][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[CH:9][C:8]([C:14]#[N:15])=[C:7]2[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:24])[F:25])[CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
A slurry of 6.00 g (16.8 mmol) of 6-nitro-4-[(3-trifluoromethylphenyl)amino]quinoline-3-carbonitrile and 18.9 g (83.3 mmol) of SnCl2 dihydrate in 240 mL of ethanol was refluxed under N2 for 1 h. After cooling to 25° C., the reaction was diluted with ice water, neutralized with sodium bicarbonate and stirred for 2 h. The product was extracted with chloroform, treated with Darco, dried(magnesium sulfate) and evaporated. The residue was filtered through silica gel (10% methanol in chloroform), evaporated and dried in vacuo (40° C.) to give 4.87 g of brown solid: mass spectrum (electrospray, m/e): M+H 329.
Workup
- extractionThe product was extracted with chloroform
- additiontreated with Darco, dried(magnesium sulfate)
- customevaporated
- filtrationThe residue was filtered through silica gel (10% methanol in chloroform)
- customevaporated
- customdried in vacuo (40° C.)
Sources & evidence
- ORD record
- ord-5cc3d37237344c81a3bd65f65ac2ae5f
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06297258B1
Reaction notes
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