반응식
[CH2:1]([NH:5][C:6]([NH2:8])=[O:7])[CH2:2][CH2:3][CH3:4].[H-].[Na+].[O:11]=[C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][N:13]1[C:21]([NH:23][CH2:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:22].[S:32](Cl)(O)(=[O:34])=[O:33]>O1CCCC1>[O:11]=[C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][N:13]1[C:21]([NH:23][CH2:24][CH2:25][C:26]1[CH:31]=[CH:30][C:29]([S:32]([NH:8][C:6]([NH:5][CH2:1][CH2:2][CH2:3][CH3:4])=[O:7])(=[O:34])=[O:33])=[CH:28][CH:27]=1)=[O:22]참가 물질
5
실험 절차
4.8 g of butyl urea are dissolved in 100 ml of tetrahydrofurane and, while stirring, 1.5 g of 80% sodium hydride (in oil) are added. The mixture is heated for 3 hours to 60° C. whereupon 7.6 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzene-sulfochloride in 100 ml of tetrahydrofurane are added while cooling. The temperature is slowly raised to 60°-70° C. and stirring is continued at that temperature for 3 hours. The solvent is removed under reduced pressure, water is added to the residue, the mixture is filtered and the filtrate is acidified with dilute hydrochloric acid. After recrystallization from dilute acetone, the N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]benzenesulfonyl)-N'-butyl-urea melts at 189°-190° C.
후처리
- additionare added
- temperaturewhile cooling
- temperatureThe temperature is slowly raised to 60°-70° C.
- stirringstirring
- customThe solvent is removed under reduced pressure, water
- additionis added to the residue
- filtrationthe mixture is filtered
- customAfter recrystallization from dilute acetone
출처 및 근거
- ORD 기록
- ord-eeaef196eedc4b268efebd985dfcd232
- 출처 데이터셋
- uspto-grants-1981_08
- 특허 번호
- US04282239
연결된 노트
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