Chloroacetaldehyde → 7-Chloro-5-methoxyimidazo[1,2-c]pyrimidine
反応式
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([O:9][CH3:10])[N:3]=1.Cl[CH2:12][CH:13]=O.C(=O)(O)[O-].[Na+].C>O.C1C=CC=CC=1>[Cl:8][C:6]1[N:5]=[C:4]([O:9][CH3:10])[N:3]2[CH:12]=[CH:13][N:1]=[C:2]2[CH:7]=1参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of 1.7 g (0.011 mole) of 4-amino-6-chloro-2-methoxypyrimidine and 3.0 g (0.015 mole) of 50% aqueous chloroacetaldehyde in 20 ml of water was heated at 80° C. for one hour, and was then cooled in an ice bath with concomitant neutralization with sodium bicarbonate. The mixture was extracted with three 50 ml portions of chloroform which were then dried over magnesium sulfate and evaporated. The residue obtained was dissolved in boiling benzene, treated with decolorizing charcoal, and filtered. The residue which was obtained by evaporation of the filtrate was triturated with diethyl ether to provide a yellow solid. The solid was purified on a preparative scale high pressure liquid chromatograph, using a mixture of 75% ethyl acetate/25% hexanes as the eluent. Recrystallization from cyclohexane gave white solid 7-chloro-5-methoxyimidazo[1,2-c]pyrimidine, m.p. 115°-118° C. Analysis: Calculated for C7H6H3OCl: %C,45.8; %H, 3.3; %N, 22.9; Found: %C, 45.4; %H, 3.1; %N, 23.4.
後処理
- extractionThe mixture was extracted with three 50 ml portions of chloroform which
- dry with materialwere then dried over magnesium sulfate
- customevaporated
- customThe residue obtained
- dissolutionwas dissolved
- filtrationfiltered
- customThe residue which was obtained by evaporation of the filtrate
- customwas triturated with diethyl ether
- customto provide a yellow solid
- customThe solid was purified on a preparative scale high pressure liquid chromatograph
- additiona mixture of 75% ethyl acetate/25% hexanes as the eluent
- customRecrystallization from cyclohexane
出典と根拠
- ORDレコード
- ord-4bda55f5a40347509669f712b959d515
- 出典データセット
- uspto-grants-1986_01
- 特許番号
- US04565864
反応ノート
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