Ethyl Acetate → 2-(2,4-Dichlorophenyl)imidazo[1,2-a]pyridine
反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.Cl[CH2:9][C:10]([C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])=O.C(OCC)(=O)C.C(=O)(O)[O-].[Na+]>C(O)C>[Cl:19][C:13]1[CH:14]=[C:15]([Cl:18])[CH:16]=[CH:17][C:12]=1[C:10]1[N:1]=[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][N:3]2[CH:9]=1参加物
実験手順
A mixture of 8.4 g (89.2 mmol) 2-aminopyridine and 20.1 g (89.9 mmol) of 2,2',4'-trichloroacetophenone in 300 ml of ethanol was heated at reflux with stirring for 14 h. At this point, another 5.0 g (22.4 mmol) of 2,2',4'-trichloroacetophenone was added and the reaction mixture heated an additional 6 h. Ethyl acetate (400 ml) and excess saturated aqueous sodium bicarbonate were slowly added. After thorough mixing, the ethyl acetate layer was separated and washed with two fold excess water, saturated brine, and dried over magnesium sulfate. Evaporating the solvent in vacuo to almost dryness gave a wet solid residue to which n-butyl chloride was added. This solid was filtered and washed thoroughly with n-butyl chloride before drying. A yield of 9.0 g of the title compound was obtained (m.p. 173-175° C.) as a technical material which was not purified further but used directly in the next step.
後処理
- temperaturewas heated
- temperatureat reflux
- temperaturethe reaction mixture heated an additional 6 h
- customAfter thorough mixing, the ethyl acetate layer was separated
- washwashed with two fold excess water, saturated brine
- dry with materialdried over magnesium sulfate
- customEvaporating the solvent in vacuo to almost dryness
- customgave a wet solid residue to which n-butyl chloride
- additionwas added
- filtrationThis solid was filtered
- washwashed thoroughly with n-butyl chloride
- custombefore drying
出典と根拠
- ORDレコード
- ord-3ac0404a8068447982d27ffe7f6b398f
- 出典データセット
- uspto-grants-1999_11
- 特許番号
- US05977028
反応ノート
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