반응식
C(O[C:4]1[CH:16]=[C:15]2[C:7]([C:8]3[CH2:9][CH2:10][CH2:11][CH2:12][C:13]=3[NH:14]2)=[CH:6][C:5]=1[C:17]([OH:19])=[O:18])C.C1(Cl)C(=O)C(Cl)=C(Cl)[C:22](=[O:23])[C:21]=1Cl.[C:32]1(C)C=CC=C[CH:33]=1>>[CH2:32]([N:14]1[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:7]2[C:15]1=[CH:16][CH:4]=[C:5]([C:17]([OH:19])=[O:18])[C:6]=2[O:23][CH2:22][CH3:21])[CH3:33]참가 물질
4
실험 절차
The 7-ethoxytetrahydrocarbazole-6-carboxylic acid obtained in Example 37 was dissolved in 8 mL of toluene, and the solution was added with 2.14 g of chloranil and refluxed for 2 hours and 30 minutes. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure and purified by silica gel column chromatography (ethyl acetate) to obtain 336 mg of 9-ethyl-5-ethoxycarbazole-6-carboxylic acid. Compound 1-38 was obtained in the same manner as in Example 36 except that the 9-ethyl-5-ethoxycarbazole-6-carboxylic acid obtained was used.
후처리
- temperaturerefluxed for 2 hours and 30 minutes
- filtrationThe reaction mixture was filtered
- concentrationthe filtrate was concentrated under reduced pressure
- custompurified by silica gel column chromatography (ethyl acetate)
출처 및 근거
- ORD 기록
- ord-bf84dbc72e724a1cb63717346ff96827
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06713473B1
연결된 노트
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