Ethanol → 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one

HRID 1578805노트

반응식

HRID 1578805 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]1

참가 물질

10

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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