Hydrochloric Acid → 1H-Imidazole, 2-(2-benzofuranyl)-1-methyl-, monohydrochloride
반응식
[ClH:1].[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH:4]=[C:3]1[C:11]1[NH:12][CH:13]=[CH:14][N:15]=1.[H-].[Na+].[CH3:18]I.Cl>CN(C=O)C.C(OCC)C.C(O)C.O>[ClH:1].[CH3:18][N:15]1[CH:14]=[CH:13][N:12]=[C:11]1[C:3]1[O:2][C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH:4]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
To a solution of the free base (7.0 g) generated from 2-(benzofuran-2-yl)imidazole hydrochloride in DMF (50 ml) at 0° C. was added sodium hydride (1.4 g) 80% in mineral oil in three equal portions. After 30 minutes at room temperature, methyl iodide (2.5 ml) was added dropwise over 15 minutes at 0° C. The mixture was then stirred for 30 minutes at room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with water and the product was extracted with hydrochloric acid (1M). The aqueous layer was basified with sodium hydroxide and the free base was extracted with ethyl acetate, washed with saturated brine and dried. Evaporation of the solvent gave a solid residue which was dissolved in diethyl ether/ethanol. Ethereal HCl was added to solution and the precipitated salt was collected by filtration (8.1 g, 91%).
후처리
- extractionextracted with ethyl acetate
- washThe organic layer was washed with water
- extractionthe product was extracted with hydrochloric acid (1M)
- extractionthe free base was extracted with ethyl acetate
- washwashed with saturated brine
- customdried
- customEvaporation of the solvent
- customgave a solid residue which
- filtrationthe precipitated salt was collected by filtration (8.1 g, 91%)
출처 및 근거
- ORD 기록
- ord-19ec5445c00f4e16a0ee0c4a8f5a4475
- 출처 데이터셋
- uspto-grants-1994_10
- 특허 번호
- US05354769
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