반응식
[CH2:1]([C@H:5]1[CH2:10][CH2:9][C@H:8]([OH:11])[CH2:7][CH2:6]1)[CH2:2][CH2:3][CH3:4].C1(C)C=CC(S(O)(=O)=O)=CC=1.[NH2:23][C:24]1([CH:49]=[CH:48][C:47]([CH2:50][CH2:51][CH2:52][CH3:53])=[CH:46][CH2:45]1)[NH:25][C:26]1[C:39]2[C:38](=[O:40])[C:37]3[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=3)[C:31](=[O:41])[C:30]=2[CH:29]=[CH:28][C:27]=1[C:42](O)=[O:43]>ClC1C=CC=CC=1Cl>[CH2:1]([C@H:5]1[CH2:6][CH2:7][C@H:8]([O:11][C:42]([C:27]2[CH:28]=[CH:29][C:30]3[C:31](=[O:41])[C:32]4[C:37](=[CH:36][CH:35]=[CH:34][CH:33]=4)[C:38](=[O:40])[C:39]=3[C:26]=2[NH:25][C:24]2([NH2:23])[CH:45]=[CH:46][C:47]([CH2:50][CH2:51][CH2:52][CH3:53])=[CH:48][CH2:49]2)=[O:43])[CH2:9][CH2:10]1)[CH2:2][CH2:3][CH3:4]참가 물질
5
실험 절차
To 200 ml of orthodichlorobenzene were added 31.6 g of trans-4-n-butylcyclohexanol, 5.6 g of p-toluenesulfonic acid, and 28 g of 1-amino-4-n-butylanilinoanthraquinone-2-carboxylic acid. The mixture was heated slowly to 110° to 115° C. and maintained at this temperature for 17 hours with stirring. The orthochlorobenzene solution was concentrated to 70 ml under reduced pressure, and 1500 ml of methanol was added. The resulting precipitates was filtered out and then purified by column chromatography wherein silica gel was used as a carrier and chloroform was used as a solvent to obtain 17.3 g of 1-amino-4-n-butylanilinoanthraquinone-2-carboxylic acid-trans-4-n-butylcyclohexyl ester.
후처리
- temperatureThe mixture was heated slowly to 110° to 115° C.
- temperaturemaintained at this temperature for 17 hours
- concentrationThe orthochlorobenzene solution was concentrated to 70 ml under reduced pressure, and 1500 ml of methanol
- additionwas added
- customThe resulting precipitates
- filtrationwas filtered out
- custompurified by column chromatography wherein silica gel
출처 및 근거
- ORD 기록
- ord-c59d58e7bcc341988eed93288b59ff2a
- 출처 데이터셋
- uspto-grants-1985_03
- 특허 번호
- US04507221
연결된 노트
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