Tetrahydrofuran → Ethyl 8-benzyl-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate
反応式
[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]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 60 °C
実験手順
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.
後処理
- temperaturethe mixture was cooled to room temperature
- filtrationfiltered
- customThe organic phase was then separated
- extractionthe aqueous phase was extracted twice with ethyl acetate
- dry with materialThe combined organic phase was dried over Na2SO4
- customevaporated
- customthe crude was purified on silica gel (eluant dichloromethane/methanol 97/3)
出典と根拠
- ORDレコード
- ord-637d3de830b24e68ae35d15e81b4357e
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08981089B2
反応ノート
読み込み中…