반응 #1095877

ord-fb635fe073c9414bb0c2d476612215a5

반응 방정식

CC1(C)CCNC1
3,3-dimethylpyrrolidine
CN(C)C=O
N,N-dimethylformamide
CC#CCOc1ncnc(Cl)c1F
4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC#CCOc1ncnc(N2CCC(C)(C)C2)c1F
4-(2-butynyloxy)-5-fluoro-6-(3,3-dimethylpyrrolidin-1-yl)pyrimidine
수율 31.7%

반응 조건

온도
80°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    온도The reaction mixture was cooled to near room temperature
  3. 3
    세척the mixture was washed with a saturated sodium chloride aqueous solution three times
  4. 4
    건조The organic layers were dried over anhydrous magnesium sulfate
  5. 5
    농축concentrated

실험 절차

Into 4 ml of N,N-dimethylformamide was resolved 0.36 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.62 g of potassium carbonate and 0.25 g of 3,3-dimethylpyrrolidine was added therein, and the mixture was stirred for 6 hours at 80° C. The reaction mixture was cooled to near room temperature, ethyl acetate was added therein, and the mixture was washed with a saturated sodium chloride aqueous solution three times. The organic layers were dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.15 g of 4-(2-butynyloxy)-5-fluoro-6-(3,3-dimethylpyrrolidin-1-yl)pyrimidine (hereinafter, referred to as Compound (28)).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07973028B2uspto-grants-2011_07