Citric Acid → 5-Methoxyacetylamino-2,4,6-triiodisophthalic acid-N,N-bis-(methoxycarbonylmethyl)-amide-chloride
반응식
[CH3:1][O:2][CH2:3][C:4]([NH:6][C:7]1[C:8]([I:21])=[C:9]([C:18](Cl)=[O:19])[C:10]([I:17])=[C:11]([C:15]=1[I:16])[C:12]([Cl:14])=[O:13])=[O:5].Cl.[CH3:23][O:24][C:25](=[O:33])[CH2:26][NH:27][CH2:28][C:29]([O:31][CH3:32])=[O:30].C(N(CC)CC)C.C(O)(=O)CC(CC(O)=O)(C(O)=O)[OH:44].C(=O)(O)[O-].[Na+]>CN(C)C=O.ClCCl.O>[Cl-:14].[CH3:32][O:31][C:29]([CH2:28][N:27]([CH2:26][C:25]([O:24][CH3:23])=[O:33])[C:18](=[O:19])[C:9]1[C:8]([I:21])=[C:7]([NH:6][C:4](=[O:5])[CH2:3][O:2][CH3:1])[C:15]([I:16])=[C:11]([C:12]([OH:44])=[O:13])[C:10]=1[I:17])=[O:30]참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
실험 절차
A solution of 66.8 g (100 mmol) of 5-methoxyacetylamino-2,4,6-triiodisophthalic acid dichloride (EP 0015867) in 300 ml of anhydrous N,N-dimethylformamide is mixed with 21.75 g (110 mmol) of iminodiacetic acid dimethyl ester-hydrochloride (synthesis according to Dubsky, Graenacher, Chem. Ber. 50, 1693 (1917)) and 30.5 ml (220 mmol) of triethylamine. A suspension results, which is stirred for 14 hours at room temperature under argon. The batch is taken up in dichloromethane, shaken out once with water, twice with 2n aqueous citric acid and once with aqueous sodium bicarbonate solution. The organic phase is dried on anhydrous magnesium sulfate and concentrated by evaporation in a vacuum. By instillation of tert-butyl ether in the concentrated solution, the title compound can be precipitated as crystalline solid, which is suctioned off and dried in a vacuum.
후처리
- customA suspension results
- dry with materialThe organic phase is dried on anhydrous magnesium sulfate
- concentrationconcentrated by evaporation in a vacuum
- customBy instillation of tert-butyl ether in the concentrated solution, the title compound can be precipitated as crystalline solid, which
- customdried in a vacuum
출처 및 근거
- ORD 기록
- ord-00d55bd08aaa4746bdd3ccdcc710804b
- 출처 데이터셋
- uspto-grants-1998_05
- 특허 번호
- US05756066
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