Thiourea → HCID 86657730, compound

HRID 1480713Notes

Reaction equation

HRID 1480713 reaction equation
Br[CH2:2][C:3]([C:5]1[C:10]([CH3:11])=[CH:9][C:8]([S:12]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)(=[O:14])=[O:13])=[CH:7][C:6]=1[CH3:23])=O.[NH2:24][C:25]([NH2:27])=[S:26]>CCO>[CH3:22][O:21][C:18]1[CH:19]=[CH:20][C:15]([S:12]([C:8]2[CH:9]=[C:10]([CH3:11])[C:5]([C:3]3[N:24]=[C:25]([NH2:27])[S:26][CH:2]=3)=[C:6]([CH3:23])[CH:7]=2)(=[O:14])=[O:13])=[CH:16][CH:17]=1

Participants

4

Procedure

A reaction mixture containing 2-bromo-1-(4-(4-methoxyphenylsulfonyl)-2,6-dimethylphenyl)ethanone (1.33 g, 3.4 mmol, 1.0 equiv) and thiourea (254.8 mg, 3.4 mmol, 1.0 equiv) in EtOH (5.0 mL) was heated at reflux for 1.0 h. The solution was concentrated under reduced pressure, and the residue was re-dissolved in EtOAc (50 mL). The solution was washed with saturated aqueous NaHCO3 (30 mL), dried over MgSO4, and concentrated under reduced pressure. The resultant solids were washed with hexanes to give 4-(4-(4-methoxyphenylsulfonyl)-2,6-dimethylphenyl)thiazol-2-amine (839.2 mg, 2.2 mmol) as yellow solids in 65% yield: 1H NMR (DMSO-d6, 500 MHz) δ 7.89 (d, J=8.9 Hz, 2H), 7.61 (s, 2H), 7.13 (d, J=8.9 Hz, 2H), 6.95 (brs, 2H), 6.43 (s, 1H), 3.83 (s, 3H), 2.16 (s, 6H); ESI-MS: m/z 375.6 (M+H)+.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 1.0 h
  3. concentrationThe solution was concentrated under reduced pressure
  4. dissolutionthe residue was re-dissolved in EtOAc (50 mL)
  5. washThe solution was washed with saturated aqueous NaHCO3 (30 mL)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. washThe resultant solids were washed with hexanes

Sources & evidence

ORD record
ord-9d0067c1a2594e4f99d3e31f54f9cfbc
Source dataset
uspto-grants-2016_08
Patent number
US09409902B2

Reaction notes

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