반응식
[C:1]([C:4]1[O:5][C:6]2[C:12]([O:13][CH2:14][CH:15]3[O:17][CH2:16]3)=[CH:11][CH:10]=[CH:9][C:7]=2[CH:8]=1)(=[O:3])[NH2:2].[ClH:18]>C(Cl)(Cl)Cl>[C:1]([C:4]1[O:5][C:6]2[C:12]([O:13][CH2:14][CH:15]([OH:17])[CH2:16][Cl:18])=[CH:11][CH:10]=[CH:9][C:7]=2[CH:8]=1)(=[O:3])[NH2:2]참가 물질
4
실험 절차
There was suspended 2.3 g of 2-carbamoyl-7-(2,3-epoxypropoxy)benzofuran obtained in Reference Example 1 in 70 ml of chloroform, and thereto 15 ml of concentrated hydrochloric acid was added. Thereafter, the mixture was vigorously stirred at room temperature for 15 minutes. After the chloroform layer was washed with water and dried with magnesium sulfate, the solvent was distilled away from the reaction mixture under reduced pressure. The resultant residue was purified by silica-gel chromatography (eluent: 2 % ethanol-chloroform) to give the desired compound.
후처리
- washAfter the chloroform layer was washed with water
- dry with materialdried with magnesium sulfate
- distillationthe solvent was distilled away from the reaction mixture under reduced pressure
- customThe resultant residue was purified by silica-gel chromatography (eluent: 2 % ethanol-chloroform)
출처 및 근거
- ORD 기록
- ord-00a4f93f0c5e423b940f80ea6c6f94fd
- 출처 데이터셋
- uspto-grants-1987_03
- 특허 번호
- US04652566
연결된 노트
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