Ethyl isothiocyanate → 1-[2-(6,8-Dichloro-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-yl)-phenyl]-3-ethyl-thiourea-Hydrochloride Salt
反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[CH2:8][N:7]([CH3:13])[CH2:6][CH:5]2[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH2:20].[N:21]([CH2:24][CH3:25])=[C:22]=[S:23]>C(#N)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[CH2:8][N:7]([CH3:13])[CH2:6][CH:5]2[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][C:22]([NH:21][CH2:24][CH3:25])=[S:23]参加物
4
実験手順
2-(6,8-Dichloro-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-yl)-phenylamine (95 mg, example 36) was dissolved in acetonitrile (4 ml) and isothiocyanato-ethane (27 mg) was added to the stirred solution. After standing for 15 h at room temperature the solvent was removed and the residue purified by preparative HPLC. The product containing fractions were combined and the acetonitrile was removed in vaccuo. After addition of potassium carbonate the aqueous phase was extracted with ethyl acetate. The organic layer was separated, dried (magnesium sulphate), filtered and concentrated in vaccuo. The residue was dissolved in water/2N hydrochloric acid and freeze dried to give 36 mg of the title compound.
後処理
- customthe solvent was removed
- customthe residue purified by preparative HPLC
- additionThe product containing fractions
- customthe acetonitrile was removed in vaccuo
- additionAfter addition of potassium carbonate the aqueous phase
- extractionwas extracted with ethyl acetate
- customThe organic layer was separated
- dry with materialdried (magnesium sulphate)
- filtrationfiltered
- concentrationconcentrated in vaccuo
- dissolutionThe residue was dissolved in water/2N hydrochloric acid
- customfreeze dried
出典と根拠
- ORDレコード
- ord-c4623bc98fec4c489798371ef2e40cab
- 出典データセット
- uspto-grants-2005_06
- 特許番号
- US06911453B2
反応ノート
読み込み中…