تفاعل #1929074

ord-4552137fdcdd4f8f81479c01df3838c4

معادلة التفاعل

Cl
hydrochloric acid
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCC(F)(F)CC1
compound
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCC(F)(F)CC1
Methyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}-4,4-difluorocyclohexanecarboxylate
CC(=O)N(C)C
DMA
CC(=O)N(C)C
DMA
CC(C)(C)[O-].[K+]
potassium tert-butoxide
Cc1ccc(Br)cc1C1=C(O)C2(CCC(F)(F)CC2)NC1=O
3-(5-Bromo-2-methylphenyl)-8,8-difluoro-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe resulting precipitate was filtered off with suction
  2. 2
    غسيلwashed with water
  3. 3
    أخرىdried in a vacuum
  4. 4
    أخرىdrying cabinet at 50° C
  5. 5
    workup.ADDITIONn-hexane was added
  6. 6
    ترشيحthe mixture was filtered off with suction
  7. 7
    أخرىdried

الإجراء التجريبي

11.0 g (27.2 mmol) of the compound from Example 10A were initially charged in a solution of 22 ml of DMA (N,N-dimethylacetamide), a solution of 10 ml of DMA and 3.54 g (1.1 eq.) of potassium tert-butoxide was added dropwise at 20-30° C. and the mixture was stirred at 30° C. for a further 1 h. The mixture was poured into 200 ml of water and the mixture was adjusted to pH 2 using aqueous 1N hydrochloric acid, the resulting precipitate was filtered off with suction, washed with water and dried in a vacuum drying cabinet at 50° C. The product was suspended in hot methyl tert-butyl ether, n-hexane was added and the mixture was filtered off with suction and dried. This gave 11.0 g (97% of theory) of the title compound in a purity of 89%.

المصدر

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