Triethylamine → 4-(5-Indanyl)-2-methylamino-5-(3-pyridyl)-1,3-thiazole
反応式
[CH3:1][NH:2][C:3]([NH2:5])=[S:4].Br.Br[CH:8]([C:20]1[CH:21]=[N:22][CH:23]=[CH:24][CH:25]=1)[C:9]([C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[CH2:16][CH2:15][CH2:14]2)=O.C(N(CC)CC)C>C(#N)C>[CH2:16]1[C:17]2[C:13](=[CH:12][C:11]([C:9]3[N:5]=[C:3]([NH:2][CH3:1])[S:4][C:8]=3[C:20]3[CH:21]=[N:22][CH:23]=[CH:24][CH:25]=3)=[CH:19][CH:18]=2)[CH2:14][CH2:15]1参加物
実験手順
In 40 ml of acetonitrile was dissolved 661 mg. of N-methyl thiourea. In the solution was suspended 2.9 g of 2-bromo-1-(5-indanyl)-2-(3-pyridyl)ethanone hydrobromide. To the suspension was added dropwise slowly 1 ml of triethylamine. The mixture was then stirred for 2 hours at refluxing temperature, followed by being left standing for cooling. The solvent was then evaporated off. To the residue was added a saturated aqueous solution of sodium hydrogen carbonate. The mixture was subjected to extraction with ethyl acetate. The extract solution was washed with water, dried and, then, the solvent was evaporated off. Recrystallization was conducted from ethyl acetate-isopropylether afforded 1.8 g (80%) of 4-(5-indanyl)-2-methylamino-5-(3-pyridyl)-1,3-thiazole, m.p. 169°-170° C.
後処理
- temperatureat refluxing temperature
- waitby being left
- temperaturefor cooling
- customThe solvent was then evaporated off
- additionTo the residue was added a saturated aqueous solution of sodium hydrogen carbonate
- extractionThe mixture was subjected to extraction with ethyl acetate
- washThe extract solution was washed with water
- customdried
- customthe solvent was evaporated off
- customRecrystallization
出典と根拠
- ORDレコード
- ord-2f4230d73f514a46bb7feb07ed4a6ccb
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04612321
反応ノート
読み込み中…