Methanol → HCID 90389409, 화합물

HRID 1526593노트

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HRID 1526593 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1.S(=O)(=O)(O)O.[CH3:17]O>>[OH:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([C:8]([O:10][CH3:17])=[O:9])=[N:6][CH:7]=1

참가 물질

4

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온도
95 °C

실험 절차

A sealable reaction vessel was charged with 5-hydroxy-3-methylpicolinic acid (0.651 g, 4.25 mmol) and MeOH (35 mL). The reaction vessel was placed in a water bath, and concentrated sulfuric acid (0.854 mL, 15.94 mmol) was added. The vessel was sealed and heated in a 95° C. oil bath. After 24 h, the reaction mixture was concentrated and the residue was taken up in 30 mL of 0.5M aqueous Na2CO3. The aqueous phase was extracted with 10% MeOH-EtOAc (100 mL). The aqueous layer was separated and saturated with NaCl. The aqueous phase was extracted with 10% MeOH-EtOAc (7×100 mL). The combined organic fractions were dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography, eluting with 3% to 4% MeOH-DCM to afford the title compound (593 mg). MS m/z=168 (M+H)+.

후처리

  1. customThe reaction vessel was placed in a water bath
  2. customThe vessel was sealed
  3. concentrationthe reaction mixture was concentrated
  4. extractionThe aqueous phase was extracted with 10% MeOH-EtOAc (100 mL)
  5. customThe aqueous layer was separated and saturated with NaCl
  6. extractionThe aqueous phase was extracted with 10% MeOH-EtOAc (7×100 mL)
  7. dry with materialThe combined organic fractions were dried over MgSO4
  8. concentrationconcentrated
  9. customThe residue was purified by silica gel chromatography
  10. washeluting with 3% to 4% MeOH-DCM

출처 및 근거

ORD 기록
ord-63c654d5b8e44620a801f696a18bec73
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09085576B2

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