Ethanol → 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one
반응식
[CH3:1][N:2]1[C:6]([C:7](Cl)=[O:8])=[C:5]([N+:10]([O-])=O)[C:4]([CH3:13])=[N:3]1.[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[OH:21].[N+]([NH-])([O-])=O.N[NH-].N1C2C=NC=N[C:31]=2[C:30](=O)N=1.Cl.[CH2:39]([N:41]([CH2:44][CH2:45]Cl)[CH2:42][CH3:43])[CH3:40].C(O)C.[O-]CC.[Na+]>C(O)(=O)C>[CH3:1][N:2]1[C:6]2[C:7](=[O:8])[N:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=3[O:21][CH2:40][CH2:39][N:41]([CH2:44][CH3:45])[CH2:42][CH3:43])[C:30]([CH3:31])=[N:10][C:5]=2[C:4]([CH3:13])=[N:3]1참가 물질
10
반응물 8
생성물 1
시약·촉매·용매 1
실험 절차
1,3-Dimethyl-4-nitro-5-pyrazolecarboxylic acid chloride is reacted with an equimolar quantity of o-aminophenol and the resulting nitroamide is catalytically reduced to the amino amide. Following the method of Example 2, the amino amide is cyclized with acetic acid in an autoclave and the resulting pyrazolopyrimidone is treated with an equimolar amount of diethylaminoethylchloride hydrochloride in absolute ethanol containing two equivalents of sodium ethoxide. 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one is obtained from the reaction mixture.
출처 및 근거
- ORD 기록
- ord-3911455a917d407eb578c6f2894bade6
- 출처 데이터셋
- uspto-grants-1976_02
- 특허 번호
- US03939161
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