Acetyl chloride → 2-Acetamido-6-aminopyridine

HRID 1591881

반응식

HRID 1591881 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[N:3]=1.[C:9](Cl)(=[O:11])[CH3:10]>O1CCOCC1>[NH2:8][C:4]1[N:3]=[C:2]([NH:1][C:9](=[O:11])[CH3:10])[CH:7]=[CH:6][CH:5]=1

참가 물질

4

반응 조건

온도
0 °C

실험 절차

Dissolve 2,6-diaminopyridine (9.822 g, 90 mmol) in dioxane (100 mL) and cool to 0° C. Add acetyl chloride (2.355 g, 2.1 mL, 30 mmol) slowly and stir for 1 hr. at 0° C. Remove the ice bath and stir at room temperature overnight. Quench the reaction mixture with saturated NaHCO3 solution, extract with ethylacetate three times. Combine the organic layers, dry over Na2SO4, filter, and concentrate to give a solid. Chromatography on silica gel, eluting with a gradient of 60–70% ethylacetate in hexanes affords the title intermediate (3.45 g, 76%): mass spectrum (ion spray): mz/z=152.1 (M+1); 1H NMR (CDCl3, ppm): 7.49 (m, 3H), 6.28 (d, 1H), 4.31 (s, br, 2H), 2.19 (s, 3H).

후처리

  1. customat 0° C
  2. customRemove the ice bath
  3. customQuench the reaction mixture with saturated NaHCO3 solution
  4. extractionextract with ethylacetate three times
  5. dry with materialCombine the organic layers, dry over Na2SO4
  6. filtrationfilter
  7. concentrationconcentrate
  8. customto give a solid
  9. washChromatography on silica gel, eluting with a gradient of 60–70% ethylacetate in hexanes

출처 및 근거

ORD 기록
ord-02e9420be8dd482db6884762f1228beb
출처 데이터셋
uspto-grants-2007_11
특허 번호
US07291632B2

연결된 노트

불러오는 중…