Citric Acid → 5-Methoxyacetylamino-2,4,6-triiodisophthalic acid-N,N-bis-(methoxycarbonylmethyl)-amide-chloride
반응식
COCC([C:6]1[C:7]([I:21])=[C:8](C(Cl)=O)[C:9]([I:17])=[C:10]([C:15]=1[I:16])[C:11]([ClH:13]N)=[O:12])=O.Cl.[CH3:23][O:24][C:25](=[O:33])[CH2:26][NH:27][CH2:28][C:29]([O:31][CH3:32])=[O:30].[CH2:34]([N:36](CC)CC)[CH3:35].C(O)(=O)C[C:43](CC(O)=O)(C(O)=O)[OH:44].[C:54](=[O:57])(O)[O-:55].[Na+].CN(C)C=[O:62]>ClCCl.O>[Cl-:13].[CH3:32][O:31][C:29]([CH2:28][N:27]([CH2:26][C:25]([O:24][CH3:23])=[O:33])[C:11](=[O:12])[C:10]1[C:15]([I:16])=[C:6]([NH:36][C:34](=[O:62])[CH2:35][O:44][CH3:43])[C:7]([I:21])=[C:8]([C:54]([OH:55])=[O:57])[C:9]=1[I:17])=[O:30]참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
A solution of 66.8 g (100 mmol) of 5-methoxyacetyl-amino-2,4,6-triiodoisophthalic acid dichloride (EP 0 015 867) 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 instilling tert-butyl ether in the concentrated solution, the title compound can precipitate 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
- customthe title compound can precipitate as crystalline solid, which
- customdried in a vacuum
출처 및 근거
- ORD 기록
- ord-09390b4a2fba4c1da8a2cce57493961f
- 출처 데이터셋
- uspto-grants-1997_01
- 특허 번호
- US05593660
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