تفاعل #1929073

ord-8a485ef6fc7e40109af79fed3c71a506

معادلة التفاعل

CCN(CC)CC
triethylamine
COC(=O)C1(N)CCC(F)(F)CC1.Cl
compound
COC(=O)C1(N)CCC(F)(F)CC1.Cl
Methyl 1-amino-4,4-difluorocyclohexanecarboxylate hydrochloride
O=S(Cl)Cl
thionyl chloride
Cc1ccc(Br)cc1CC(=O)O
(5-bromo-2-methylphenyl)acetic acid
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCC(F)(F)CC1
Methyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}-4,4-difluorocyclohexanecarboxylate

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 100 ml of tetrahydrofuran (THF) (solution A)
  3. 3
    درجة الحرارةwith cooling
  4. 4
    workup.STIRRINGthe mixture was stirred at room temperature until the reaction
  5. 5
    ترشيحThe precipitate is filtered off with suction
  6. 6
    غسيلwashed with THF
  7. 7
    تركيزthe filtrate is concentrated under reduced pressure
  8. 8
    أخرىthe residue is recrystallized from methyl tert-butyl ether

الإجراء التجريبي

36.5 ml (500 mmol) of thionyl chloride were added to 22.91 g (100 mmol) of (5-bromo-2-methylphenyl)acetic acid (EP 1791816 A1 and WO 2006/29799 A1), and the mixture was stirred at 80° C. until the evolution of gas was complete and then concentrated. The residue was dissolved in 100 ml of tetrahydrofuran (THF) (solution A). 25.3 g (110 mmol) of the compound from Example 4A were initially charged in 308 ml of THF, 21.3 ml of triethylamine were added dropwise at 20° C., solution A was then added dropwise with cooling and the mixture was stirred at room temperature until the reaction had gone to completion. The precipitate is filtered off with suction and washed with THF, the filtrate is concentrated under reduced pressure and the residue is recrystallized from methyl tert-butyl ether. This gave 33.6 g (83% of theory) of the title compound.

المصدر

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