Hydrochloric Acid → 6-cyclopentyl-4H-isoquinoline-1,3-dione

HRID 2236452노트

반응식

HRID 2236452 반응식
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([O:12][Si](C(C)(C)C)(C)C)=[N:7][C:6]([O:20][Si](C(C)(C)C)(C)C)=[CH:5]2.[CH:28]1([Mg]Br)[CH2:32][CH2:31][CH2:30][CH2:29]1.CCOCC.Cl>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O.C1COCC1>[CH:28]1([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[C:8](=[O:12])[NH:7][C:6](=[O:20])[CH2:5]3)[CH2:32][CH2:31][CH2:30][CH2:29]1

참가 물질

8

실험 절차

To 6-bromo-1,3-bis-(tert-butyl-dimethyl-silanyloxy)-isoquinoline (1.76 g, 3.75 mmole) is added tetrakis(triphenylphosphine)palladium (110 mg, 0.095 mmole) and 2M cyclopentyl magnesium bromide in ether (3.0 mL, 6.0 mmole). This mixture is heated using a microwave reactor at 75° C. for 600 sec. The mixture is cooled to room temperature, transferred to a flask with THF and water, then 2M hydrochloric acid (20 mL) is added and stirred for 4 hours at room temperature. The organic solvents were removed in vacuo, the mixture extracted with ethyl acetate, the organic layer dried over sodium sulfate filtered, evaporated and chromatographed with hexanes-ethyl acetate on silica gel to give a white solid, 268 mg (31%) MS (ESI): m/z 230.2 (M+H).

후처리

  1. temperatureThis mixture is heated
  2. customat 75° C.
  3. customfor 600 sec
  4. customThe organic solvents were removed in vacuo
  5. extractionthe mixture extracted with ethyl acetate
  6. dry with materialthe organic layer dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customchromatographed with hexanes-ethyl acetate on silica gel
  10. customto give a white solid, 268 mg (31%)

출처 및 근거

ORD 기록
ord-ce4394cef63c46729cae2d156b479e39
출처 데이터셋
uspto-grants-2010_05
특허 번호
US07713994B2

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