تفاعل #2157072

ord-a3bd1b1c6a4042ad87b95e5d834552ad

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىTo a mixture obtained
  2. 2
    workup.ADDITIONis added dropwise at 25 to 30° C. over one hour
  3. 3
    workup.STIRRINGby stirring
  4. 4
    workup.STIRRINGafter the mixture is stirred at 30° C.
  5. 5
    أخرىAfter separating into the organic layer
  6. 6
    أخرىthe aqueous layer, the aqueous layer is removed
  7. 7
    غسيلthe organic layer is washed once with 220.0 g of 5% hydrochloric acid
  8. 8
    غسيلwashed once with 220.0 g of water
  9. 9
    تركيزThe organic layer is concentrated

الإجراء التجريبي

To a mixture obtained by adding 110.0 g of 4,5,6-trifluoropyrimidine, 114.6 g of potassium carbonate and 16.6 g of triethylamine to 220.0 g of toluene, 60.4 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 85.4 g of 3,3-dimethylpyrrolidine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 4-(2-butynyloxy)-5-fluoro-6-(3,3-dimethylpyrrolidin-1-yl)pyrimidine (hereinafter referred to as the present compound (1)).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08299245B2uspto-grants-2012_10