تفاعل #1929075

ord-d7222d60a7b1471f8cbe6eb4fc08638e

معادلة التفاعل

CCN(CC)CC
triethylamine
COC(=O)C1(N)CCCCC1.Cl
methyl 1-aminocyclohexanecarboxylate hydrochloride
Cc1ccc(Br)cc1CC(=O)O
(5-bromo-2-methylphenyl)acetic acid
O=S(Cl)Cl
thionyl chloride
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCCCC1
Methyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}cyclohexanecarboxylate

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in 20 ml of dichloromethane
  3. 3
    workup.STIRRINGthe mixture was stirred at room temperature for 0.5 h
  4. 4
    workup.STIRRINGthe mixture was stirred at room temperature for 36 h
  5. 5
    workup.ADDITIONThe mixture was then diluted
  6. 6
    غسيلwashed with water, 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution
  7. 7
    أخرىdried
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated

الإجراء التجريبي

2.06 g (9.00 mmol) of (5-bromo-2-methylphenyl)acetic acid (described in EP 1791816 and WO 2006/29799) were dissolved in 3.7 ml (51.3 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for 2 h and then concentrated. The residue was dissolved in 20 ml of dichloromethane. 2.09 g (10.8 mmol) of methyl 1-aminocyclohexanecarboxylate hydrochloride were dissolved in 25 ml of dichloromethane, 55 mg (0.45 mmol) of 4-dimethylaminopyridine and 3.1 ml (22.5 mmol) of triethylamine were added and the mixture was stirred at room temperature for 0.5 h. The solution of the acid chloride was added dropwise, and the mixture was stirred at room temperature for 36 h. The mixture was then diluted with diluted with dichloromethane, washed with water, 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution, dried, filtered and concentrated. This gave 2.80 g (84% of theory) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08946124B2uspto-grants-2015_02