반응 #435681

ord-e271941b58034d948f098e0d38073e31

반응 방정식

CO
Methanol
Nc1ccccc1Nc1ccccc1
N-phenyl-benzene-1,2-diamine
CSc1ncc(C(=O)Nc2ccc(F)cc2)c(Cl)n1
4-chloro-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide
CN1CCOCC1
N-methylmorpholine
CSc1ncc(C(=O)Nc2ccc(F)cc2)c(Nc2ccccc2Nc2ccccc2)n1
titled compound
수율 47.1%
CSc1ncc(C(=O)Nc2ccc(F)cc2)c(Nc2ccccc2Nc2ccccc2)n1
2-Methylsulfanyl-4-(2-(phenylamino)phenylamino)pyrimidine-5-carboxylic acid (4-fluorophenyl)amide
수율 47.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was then heated
  2. 2
    온도at reflux for an additional 2 h
  3. 3
    workup.STIRRINGthe mixture was stirred at an ambient temperature for 40 h
  4. 4
    여과The mixture was filtered through a plug of celite
  5. 5
    세척the filter plug was washed with hot ethyl acetate (25 mL)
  6. 6
    workup.ADDITIONThe resulting solution was treated with hexanes

실험 절차

To a mixture of 4-chloro-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide (100 mg, 0.34 mmol) in dichloromethane (10 mL) was added N-phenyl-benzene-1,2-diamine (148 mg, 0.4 mmol) followed by N-methylmorpholine-bound resin (300 mg). The mixture was stirred at an ambient temperature for 16 h and was then heated at reflux for an additional 2 h. Methanol (5 mL) was added and the mixture was stirred at an ambient temperature for 40 h. The mixture was filtered through a plug of celite and the filter plug was washed with hot ethyl acetate (25 mL). The resulting solution was treated with hexanes to precipitate 70 mg (0.16 mmol, 47% yield) of the titled compound as a purple-red solid. 1H NMR (300 MHz, DMSO-d6) δ 10.64 (s, 1H), 10.29 (s, 1H), 8.74 (s, 1H), 8.10 (m, 1H), 7.58 (m, 3H), 7.25–7.05 (m, 7H), 6.79–6.679(m, 3H), 2.5(s, 3H); MS (EI) m/z 444.05 (M−H)−.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07176310B1uspto-grants-2007_02