Citric Acid → N-(4-azido-2-nitrophenyl)-N'-(N-((2-hydroxyethyldithio)-2-ethylamidosuccinimido)-3-aminopropyl)-N'-methyl-1,3-propanediamine citrate salt
반응식
[N:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][CH2:12][CH2:13][N:14]([CH2:16][CH2:17][CH2:18][NH:19][N:20]2[C:24](=[O:25])[CH2:23][CH:22]([NH:26][C:27](=[O:34])[CH2:28][S:29][S:30][CH2:31][CH2:32][OH:33])[C:21]2=[O:35])[CH3:15])=[C:6]([N+:36]([O-:38])=[O:37])[CH:5]=1)=[N+:2]=[N-:3].[C:39]([OH:51])(=[O:50])[CH2:40][C:41]([CH2:46][C:47]([OH:49])=[O:48])([C:43]([OH:45])=[O:44])[OH:42]>CO>[C:39]([OH:51])(=[O:50])[CH2:40][C:41]([CH2:46][C:47]([OH:49])=[O:48])([C:43]([OH:45])=[O:44])[OH:42].[N:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][CH2:12][CH2:13][N:14]([CH2:16][CH2:17][CH2:18][NH:19][N:20]2[C:24](=[O:25])[CH2:23][CH:22]([NH:26][C:27](=[O:34])[CH2:28][S:29][S:30][CH2:31][CH2:32][OH:33])[C:21]2=[O:35])[CH3:15])=[C:6]([N+:36]([O-:38])=[O:37])[CH:5]=1)=[N+:2]=[N-:3]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
The reaction was carried out in the dark. A flask charged with a solution of 1.15 g (2.12 mmole) of N-(4-azido-2-nitrophenyl)-N'-(N-((2-hydroxyethyldithio)-2-ethylamidosuccinimido) -3-aminopropyl)-N'-methyl-1,3-propanediamine in a minimal amount of methanol was treated with a solution of 407.1 mg (2.12 mmole) citric acid dissolved in a minimal amount of methanol at room temperature. After stirring for 5 min the volatiles where removed in vacuo to give 1.4027 g of the desired product as a red solid.
후처리
- customremoved in vacuo
출처 및 근거
- ORD 기록
- ord-3a9f5c6b59fb4143b36742fc5a8e953a
- 출처 데이터셋
- uspto-grants-1997_12
- 특허 번호
- US05700921
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