Hydrochloric Acid → 1-[(1,3-Thiazol-2-yl)methyl]-1,3-dihydro-2H-imidazole-2-thione
反応式
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=O.C(O[CH:11](OCC)[CH2:12][NH2:13])C.CC1C=CC(S(O)(=O)=O)=CC=1.[BH4-].[Na+].[C:30]([S-:32])#[N:31].[K+].Cl>C(O)C.O>[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH2:6][N:13]1[CH:12]=[CH:11][NH:31][C:30]1=[S:32]参加物
9
反応物 6
生成物 1
試薬・触媒・溶媒 2
実験手順
In a 500 ml round bottom blask is placed 6 g (0.053 mol) 2-thiazolecarboxaldehyde, 7.0 g (0.053 mol) aminoacetaldehyde diethylacetal, 0.1 g TsOH and 150 ml ethanol. The reaction is refluxed 2 hours, cooled and concentrated. The residue is redissolved in 200 ml ethanol and 2.3 g (0.06 mol) NaBH4 added. The reaction is refluxed 4 hours then poured onto 500 ml water. The amino derivative is extracted into CH2Cl2 (2×100 ml), dried (Na2SO4) and concentrated to give an orange oil. The entire product is dissolved in 200 ml ethanol and 5.1 g (0.053 mol) KSCN, 30 ml water and 8 ml concentrated HCl added. The reaction is refluxed for 6 hours, cooled and then poured onto 1 liter ice water. The tan solid is collected and dried.
後処理
- temperatureThe reaction is refluxed 2 hours
- temperaturecooled
- concentrationconcentrated
- dissolutionThe residue is redissolved in 200 ml ethanol
- temperatureThe reaction is refluxed 4 hours
- extractionThe amino derivative is extracted into CH2Cl2 (2×100 ml)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customto give an orange oil
- temperatureThe reaction is refluxed for 6 hours
- temperaturecooled
- customThe tan solid is collected
- customdried
出典と根拠
- ORDレコード
- ord-0cbeebf686b54534aa6109a80dbc853f
- 出典データセット
- uspto-grants-1989_03
- 特許番号
- US04810800
反応ノート
読み込み中…