Thiourea → HCID 58442442, compound

HRID 1480691Notes

Reaction equation

HRID 1480691 reaction equation
Br[CH2:2][C:3]([C:5]1[C:10]([CH3:11])=[CH:9][C:8]([O:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH3:20])[CH:14]=2)=[CH:7][C:6]=1[CH3:21])=O.[NH2:22][C:23]([NH2:25])=[S:24]>CCO>[CH3:20][O:19][C:15]1[CH:14]=[C:13]([CH:18]=[CH:17][CH:16]=1)[O:12][C:8]1[CH:9]=[C:10]([CH3:11])[C:5]([C:3]2[N:22]=[C:23]([NH2:25])[S:24][CH:2]=2)=[C:6]([CH3:21])[CH:7]=1

Participants

4

Reactant 2

HCID 2723790ThioureaHCID 58442432HCID 58442432, compound

Product 1

HCID 58442442HCID 58442442, compoundYield 65.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 2-bromo-1-(4-(3-methoxyphenoxy)-2,6-dimethylphenyl)ethanone (6.98 g, 20.0 mmol) and thiourea (1.52 g, 20.0 mmol) in 95% EtOH (28.5 mL) was heated at reflux for 5.0 h. The solution was concentrated and added with water (50 mL) and saturated aqueous Na2CO3 (1.0 mL), and extracted with ethyl acetate (100 ml). The organic layer was washed with brine, dried over anhydrous MgSO4(s), and concentrated under reduced pressure to give 4-(4-(3-methoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-amine (4.30 g) as deep-brown oil, which was used directly for the next step without further purification.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 5.0 h
  3. concentrationThe solution was concentrated
  4. additionadded with water (50 mL) and saturated aqueous Na2CO3 (1.0 mL)
  5. extractionextracted with ethyl acetate (100 ml)
  6. washThe organic layer was washed with brine
  7. dry with materialdried over anhydrous MgSO4(s)
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-f46f5420ee854e288c82f47968dd59ba
Source dataset
uspto-grants-2016_08
Patent number
US09409902B2

Reaction notes

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