3-Butyn-2-amine, 2-methyl- → HCID 13131825、化合物
反応式
[C:1]([C:3]1[CH:14]=[C:13]([NH:15][C:16]([CH:18]2[CH2:21][CH2:20][CH2:19]2)=[O:17])[CH:12]=[CH:11][C:4]=1[O:5][CH2:6][CH:7]([OH:10])[CH2:8]Cl)#[N:2].[CH3:22][C:23]([NH2:27])([C:25]#[CH:26])[CH3:24]>C(O)C>[C:1]([C:3]1[CH:14]=[C:13]([NH:15][C:16]([CH:18]2[CH2:21][CH2:20][CH2:19]2)=[O:17])[CH:12]=[CH:11][C:4]=1[O:5][CH2:6][CH:7]([OH:10])[CH2:8][NH:27][C:23]([CH3:24])([C:25]#[CH:26])[CH3:22])#[N:2]参加物
実験手順
7.5 gm (0.024 mol) of 1-(2-cyano-4-cyclobutylcarbonylamino-phenoxy)-2-hydroxy-3-chloro-propane were dissolved in 20 ml of ethanol, 8.3 gm (0.1 mol) of 2-methyl-but-3-in-2-yl-amine were added to the solution, and the mixture was refluxed for 3.5 hours. The ethanol was then distilled off, and the residue was digested with H2O. After being acidified with HCl, the mixture was washed with ether, the acidic aqueous phase was made alkaline with NH4OH, and the base precipitated thereby was extracted by shaking twice with ethyl acetate. The organic phase was washed with H2O, dried over MgSO4 and the ethyl acetate was distilled off in vacuo. The crystalline residue (base) was recrystallized twice from acetonitrile, and 3.7 gm of pure substance were obtained. Melting point: 139°-141° C.
後処理
- temperaturethe mixture was refluxed for 3.5 hours
- distillationThe ethanol was then distilled off
- washthe mixture was washed with ether
- customthe base precipitated
- extractionthereby was extracted
- washThe organic phase was washed with H2O
- dry with materialdried over MgSO4
- distillationthe ethyl acetate was distilled off in vacuo
- customThe crystalline residue (base) was recrystallized twice from acetonitrile, and 3.7 gm of pure substance
- customwere obtained
出典と根拠
- ORDレコード
- ord-a751584f4af74c9796c0416687464c44
- 出典データセット
- uspto-grants-1984_04
- 特許番号
- US04442121
反応ノート
読み込み中…