Tetrahydrofuran → Ethyl 8-benzyl-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

HRID 875086노트

반응식

HRID 875086 반응식
[Br-].[CH2:2]([Zn+])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C1COCC1.[CH3:15][N:16]1[C:28]2[C:27]3[N:26]=[C:25](SC)[N:24]=[CH:23][C:22]=3[CH2:21][CH2:20][C:19]=2[C:18]([C:31]([O:33][CH2:34][CH3:35])=[O:32])=[N:17]1.C(=O)(O)[O-].[Na+]>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.C(OCC)(=O)C>[CH2:2]([C:25]1[N:24]=[CH:23][C:22]2[CH2:21][CH2:20][C:19]3[C:18]([C:31]([O:33][CH2:34][CH3:35])=[O:32])=[N:17][N:16]([CH3:15])[C:28]=3[C:27]=2[N:26]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

참가 물질

7

반응 조건

온도
60 °C

실험 절차

Under a nitrogen atmosphere, a 0.5 M solution of benzylzinc bromide in THF (3.11 mL, 1.556 mmol) was added to a mixture of ethyl 1-methyl-8-(methylthio)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (237 mg, 0.778 mmol) and Pd(PPh3)4 (9 mg, 0.0078 mmol, 1%). After 20 hours of heating at 60° C. under nitrogen, the mixture was cooled to room temperature, shaken with aqueous sodium bicarbonate and ethyl acetate and then filtered. The organic phase was then separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic phase was dried over Na2SO4, evaporated and the crude was purified on silica gel (eluant dichloromethane/methanol 97/3). 20 mg of the title compound were isolated.

후처리

  1. temperaturethe mixture was cooled to room temperature
  2. filtrationfiltered
  3. customThe organic phase was then separated
  4. extractionthe aqueous phase was extracted twice with ethyl acetate
  5. dry with materialThe combined organic phase was dried over Na2SO4
  6. customevaporated
  7. customthe crude was purified on silica gel (eluant dichloromethane/methanol 97/3)

출처 및 근거

ORD 기록
ord-637d3de830b24e68ae35d15e81b4357e
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08981089B2

반응 노트

불러오는 중…