m-Toluidine → 6-Nitro-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrile

HRID 1934986Notes

Reaction equation

HRID 1934986 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:15]#[N:16].[NH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=1.C(=O)(O)[O-].[Na+]>C(O)C>[N+:12]([C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]=[CH:4][C:3]([C:15]#[N:16])=[C:2]2[NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=1)([O-:14])=[O:13]

Participants

5

Reactant 3

HCID 7934m-ToluidineHCID 516892Sodium BicarbonateHCID 110856904-Chloro-6-nitroquinoline-3-carbonitrile

Product 1

HCID 224665426-Nitro-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrileYield 73.7%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 5.00 g (21.5 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile, 200 ml ethanol, and 2.75 ml (25.7 mmol) 3-toluidine was heated to reflux for 4.5 hours. Cooled and added a saturated sodium bicarbonate until pH was basic. Stripped solvents and azeotroped with ethanol. Slurried with hexane, collected, and air dried. Washed with water and dried in vacuo. Boiled in ethyl acetate, stirred with Darco and filtered. Stripped solvent and dried in vacuo to give 4.82 g of yellow-orange solid: mass spectrum (electrospray m/e): M+H=305.2.

Workup

  1. temperaturewas heated
  2. temperatureto reflux for 4.5 hours
  3. temperatureCooled
  4. customStripped solvents and azeotroped with ethanol
  5. customSlurried with hexane, collected
  6. customair dried
  7. washWashed with water
  8. customdried in vacuo
  9. filtrationfiltered
  10. customStripped solvent and dried in vacuo

Sources & evidence

ORD record
ord-33f51bfd93ea4e80aba1bfe736220f7a
Source dataset
uspto-grants-2002_05
Patent number
US06384051B1

Reaction notes

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