3-Bromo-o-toluidine → HCID 59375104, compound

HRID 1811051Notes

Reaction equation

HRID 1811051 reaction equation
[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].F[C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][N:12]=1.CC(C)([O-])C.[K+]>CS(C)=O>[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([NH:5][C:11]2[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][N:12]=2)[CH:6]=[CH:7][CH:8]=1

Participants

5

Reactant 3

HCID 1235383-Bromo-o-toluidineHCID 27374032-Fluoro-4-methylpyridineHCID 23665647Potassium tert-butoxide

Product 1

HCID 59375104HCID 59375104, compoundYield 34%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
190 °C

Procedure

A mixture of 3-bromo-2-methylaniline (200 mg, 1.075 mmol), 2-fluoro-4-methylpyridine (155 mg, 1.397 mmol) and potassium tert-butoxide (193 mg, 1.72 mmol) in DMSO (4 mL) was heated in a sealed tube via microwave irradiation at 190° C. for 40 min. The mixture was partitioned between EtOAc and water, and the organic phase was washed with brine, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from hexane to 85:15 hexane-EtOAc) to provide N-(3-bromo-2-methylphenyl)-4-methylpyridin-2-amine as a yellow solid (100 mg, 34%). 1H NMR (400 MHz, chloroform-d) δ 8.05 (1H, d, J=5.3 Hz), 7.38 (2H, d, J=8.1 Hz), 7.06 (1H, t, J=8.0 Hz), 6.58 (1H, d, J=5.3 Hz), 6.40 (1H, s), 6.23 (1H, br. s.), 2.37 (3H, s), 2.23 (3H, s). Mass spectrum m/z 277, 279 (M+H)+.

Workup

  1. customThe mixture was partitioned between EtOAc and water
  2. washthe organic phase was washed with brine
  3. customdried
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography (
  6. washeluting with a gradient from hexane to 85:15 hexane-EtOAc)

Sources & evidence

ORD record
ord-52633c55b0cb4991bf89146636d97af3
Source dataset
uspto-grants-2013_01
Patent number
US08362065B2

Reaction notes

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