Tetrahydrofuran → 4-Methoxy-2-(2-methyl-[1,3]-dioxolan-2-yl)benzoxazole-7-carboxylic acid

HRID 275805노트

반응식

HRID 275805 반응식
Br[C:2]1[C:10]2[O:9][C:8]([C:11]3([CH3:16])[O:15][CH2:14][CH2:13][O:12]3)=[N:7][C:6]=2[C:5]([O:17][CH3:18])=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C.[C]=[O:56].[O:57]1[CH2:61]CCC1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[CH3:18][O:17][C:5]1[C:6]2[N:7]=[C:8]([C:11]3([CH3:16])[O:15][CH2:14][CH2:13][O:12]3)[O:9][C:10]=2[C:2]([C:61]([OH:57])=[O:56])=[CH:3][CH:4]=1

참가 물질

8

실험 절차

7-Bromo-4-methoxy-2-(2-methyl-[1,3]-dioxolan-2-yl)benzoxazole (480 mg), palladium acetate (34 mg), 1,3-bis(diphenylphosphino)propane (126 mg), triethylamine (0.21 ml), water (15 ml) and tetrahydrofuran (30 ml) were combined and heated to 90° C. in a Parr apparatus under 1035 kPa (150 psi) of carbon monoxide for 3 days. After cooling to room temperature, the tetrahydrofuran was evaporated in vacuo. The residue was partitioned between ethyl acetate (50 ml) and water (50 ml). The aqueous layer was extracted with ethyl acetate (50 ml). The combined organic extracts were dried over magnesium sulphate, evaporated in vacuo and purified by flash chromatography eluting with ethyl acetate to yield the title compound as a white solid (190 mg).

후처리

  1. customthe tetrahydrofuran was evaporated in vacuo
  2. customThe residue was partitioned between ethyl acetate (50 ml) and water (50 ml)
  3. extractionThe aqueous layer was extracted with ethyl acetate (50 ml)
  4. dry with materialThe combined organic extracts were dried over magnesium sulphate
  5. customevaporated in vacuo
  6. custompurified by flash chromatography
  7. washeluting with ethyl acetate

출처 및 근거

ORD 기록
ord-c26c330d25cb49308191857aa8d3dfd8
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06353010B1

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