Triethylamine → 2-Ethylthio-5-(hex-5-ynylaminocarbonyl)thiazole
反応式
[CH2:1]([S:3][C:4]1[S:5][C:6]([C:9]([OH:11])=O)=[CH:7][N:8]=1)[CH3:2].C(N(CC)CC)C.C(OC(Cl)=O)C.[NH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]#[CH:31]>O1CCCC1>[CH2:1]([S:3][C:4]1[S:5][C:6]([C:9]([NH:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]#[CH:31])=[O:11])=[CH:7][N:8]=1)[CH3:2]参加物
反応条件
- 温度
- -30 °C
実験手順
In this preparation 0.1 mole of 2-ethylthio-5-carboxythiazole is dissolved in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, and 0.1 moles of triethylamine is added and the resulting mixture cooled to -30° C. 0.1 Mole of ethylchloroformate is then added dropwise with stirring and the resulting mixture allowed to warm to 0° C. The mixture is then stirred for ten minutes, then cooled to -30° C and 0.11 mole of 1-aminohex-5-yne in 50 ml. of tetrahydrofuran added dropwise. The mixture is allowed to warm to room temperature (about 20° C), poured into 500 ml. of ethyl acetate, washed with water, then washed with saturated aqueous sodium chloride solution, and dried over magnesium sulfate. The mixture is then filtered and the solvent from the resulting filtrate is evaporated under vacuum yielding 2-ethylthio-5-(hex-5-ynylaminocarbonyl)thiazole as a solid, which is then further purified by recrystallization from ethyl acetate.
後処理
- dissolutionis dissolved in 300 ml
- temperatureto warm to 0° C
- stirringThe mixture is then stirred for ten minutes
- temperaturecooled to -30° C
- temperatureto warm to room temperature (about 20° C)
- additionpoured into 500 ml
- washof ethyl acetate, washed with water
- washwashed with saturated aqueous sodium chloride solution
- dry with materialdried over magnesium sulfate
- filtrationThe mixture is then filtered
- customthe solvent from the resulting filtrate is evaporated under vacuum
出典と根拠
- ORDレコード
- ord-7e7cf0700a6e44f584edd7c08177ae9f
- 出典データセット
- uspto-grants-1977_12
- 特許番号
- US04064257
反応ノート
読み込み中…