Phosphorus oxychloride → 6-Methyl-N,N-dicyclopentylnicotinamide

HRID 981053

반응식

HRID 981053 반응식
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][N:3]=1.[CH:11]1([NH:16][CH:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH2:15][CH2:14][CH2:13][CH2:12]1.P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:16]([CH:17]2[CH2:18][CH2:19][CH2:20][CH2:21]2)[CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15]2)=[O:8])=[CH:4][N:3]=1

참가 물질

5

실험 절차

To a suspension of 6-methylnicotinic acid (1.37 g, 10 mmol) in toluene (10 ml), N,N-dicyclopentylamine (1.84 g, 12 mmol) was added To the homogenous solution obtained, phosphorus oxychloride (0.23 mL, 12 mmol) was injected in dropwise fashion. The reaction mixture was then immersed in an oil-bath at 130° C. and refluxed for 8 h. The reaction flask was cooled and stirred at room temperature. After 16h, the reaction was quenched with water and extracted in ethyl acetate. The organic layer was successively washed with aq. potassium carbonate, water and brine. After drying (MgSO4), the solvent was removed. The crude product (2.5 g) was chromatographed (silica gel, ethyl acetate/acetonitrile 100/1.5) to give the title compound (1.2 g, 44%). IR (KBr)1625, 1590, 1450, 1430, 1375, 1340, 1290, 1130, 840, 750 cm-1 ; 1H NMR (CDCl3) 1.4-2.35 (m, 16H), 2.57 (s, 3H), 3.6-3.9 (m,2H), 7.17 (d, J=8 Hz, 1H), 7.6 (dd,J=3,8 Hz, 1H), and 8.5 ppm (d,J=3 Hz,1H).

후처리

  1. additionwas added To the homogenous solution
  2. customobtained
  3. customThe reaction mixture was then immersed in an oil-bath at 130° C.
  4. temperaturerefluxed for 8 h
  5. temperatureThe reaction flask was cooled
  6. customAfter 16h, the reaction was quenched with water
  7. extractionextracted in ethyl acetate
  8. washThe organic layer was successively washed with aq. potassium carbonate, water and brine
  9. dry with materialAfter drying (MgSO4)
  10. customthe solvent was removed
  11. customThe crude product (2.5 g) was chromatographed (silica gel, ethyl acetate/acetonitrile 100/1.5)

출처 및 근거

ORD 기록
ord-e957701b38974072ae9583c99c4acedf
출처 데이터셋
uspto-grants-1991_02
특허 번호
US04990518

연결된 노트

불러오는 중…