Sodium Chloride → HCID 20186089, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([NH:8][CH:9]([CH2:13][CH:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][C:15]2=O)[C:10]([OH:12])=[O:11])=[O:7])=[CH:4][CH:3]=1.[NH2-].[Na+].[CH2:28](Cl)[CH:29]=[CH2:30].[Cl-].[Na+].CN(C)C=[O:37]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:8][CH:9]([CH2:13][C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([O:37][CH2:28][CH:29]=[CH2:30])[CH:15]=2)[C:10]([OH:12])=[O:11])=[O:7])=[CH:24][CH:25]=1Komponenten
Versuchsvorschrift
479 Milligrams of 2-(4-chlorobenzoylamino)-3-(oxindol-3-yl)propionic acid 1/4-hydrate prepared in Example 3 and 0.05 g of sodium amide were admixed in 5 ml of dimethylformamide, and the mixture was stirred at a room temperature for 2 hours. Then 0.17 g of allyl chloride was added to the mixture and the resulting reaction mixture was stirred at a room temperature for 10 hours. The reaction mixture was poured into 13 ml of a saturated sodium chloride aqueous solution, and the organic material was extracted with chloroform. The chloroform layer was washed with water, dried, then chloroform was removed by evaporation. The residure thus obtained was purified by means of a silica gel column chromatography to yield 85 mg of 2-(4-chlorobenzoylamino)-3-(1-allyloxyindol-3-yl)propionic acid.
Aufarbeitung
- customthe resulting reaction mixture
- stirringwas stirred at a room temperature for 10 hours
- extractionthe organic material was extracted with chloroform
- washThe chloroform layer was washed with water
- customdried
- customchloroform was removed by evaporation
- customThe residure thus obtained
- customwas purified by means of a silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-9515d0a1b4914cecab75dcf208c2d7cc
- Quelldatensatz
- uspto-grants-1987_09
- Patentnummer
- US04694017
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