Bromine → 4,6-Dibromothiazolo[5,4-c]pyridin-2-amine

HRID 447066노트

반응식

HRID 447066 반응식
[Br:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]([NH2:11])=[S:10])[CH:5]=[C:4]([Br:12])[N:3]=1.BrBr>C1COCC1>[Br:1][C:2]1[C:7]2[S:10][C:9]([NH2:11])=[N:8][C:6]=2[CH:5]=[C:4]([Br:12])[N:3]=1

참가 물질

4

반응 조건

온도
2.5 °C

실험 절차

To a cooled (−60-65° C.) solution of 2,6-dibromo-pyridin-4-yl-thiourea (0.50 g, 1.61 mmol) in THF (100 mL) was added bromine solution (0.20 mL in 45 mL THF, 3.69 mmol) drop wise over a period of 30 min maintaining the temperature to −60-65° C. The reaction mixture was stirred for 15 min at the same temperature and then slowly allowed to come to room temperature. The resulting mixture was heated up to 40° C. for 5 h. After completion of reaction (TLC monitoring), THF was distilled off, basified with aq. NH3 (25% solution, pH 10-12) and then extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (100-200 M, 10% ethyl acetate:hexane) to get the desired product as a white solid (0.10 g, 20%).

후처리

  1. customto come to room temperature
  2. temperatureThe resulting mixture was heated up to 40° C. for 5 h
  3. distillationwas distilled off
  4. extractionextracted with ethyl acetate (3×50 mL)
  5. washThe combined organics was washed with water
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude residue was purified over silica gel (100-200 M, 10% ethyl acetate:hexane)

출처 및 근거

ORD 기록
ord-7daa89b30327451db42a391c9e987bf7
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08481544B2

반응 노트

불러오는 중…