반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8](O)=[O:9])([CH3:4])([CH3:3])[CH3:2].ON1C(=O)CCC1=O.Cl.C(N=C=NCCCN(C)C)C.[NH2:39][CH2:40][CH2:41][CH2:42][S:43][C:44]1[CH:49]=[CH:48][N:47]=[CH:46][CH:45]=1>C(Cl)Cl>[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:16])([CH3:18])[CH3:17])[C:13]=1[OH:14])[C:8]([NH:39][CH2:40][CH2:41][CH2:42][S:43][C:44]1[CH:49]=[CH:48][N:47]=[CH:46][CH:45]=1)=[O:9])([CH3:2])([CH3:3])[CH3:4]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 1.49 g (5.94 mmol) of 3,5-di-t-butyl-4-hydroxybenzoic acid and 889 mg (7.73 mmol) of N-hydroxysuccinimide in 60 ml of methylene chloride was added 1.38 g (7.13 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. Further 1.00 g (5.94 mmol) of 4-(3-aminopropylthio)pyridine was added and the mixture was stirred at room temperature for 8 hours. The reaction mixture was washed with water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 650 mg of the desired compound (27.3%, colorless powder) mp: 203.0°-204.0° C.
후처리
- temperaturecooling
- stirringthe mixture was stirred at room temperature for 30 minutes
- stirringthe mixture was stirred at room temperature for 8 hours
- washThe reaction mixture was washed with water
- customdried
- distillationThe solvent was distilled off
- customThe residue was purified by column chromatography (eluent: ethyl acetate)
출처 및 근거
- ORD 기록
- ord-42ff702e697f47449de28e810a22d33c
- 출처 데이터셋
- uspto-grants-1996_10
- 특허 번호
- US05561147
연결된 노트
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