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Sodium Bicarbonate → HCID 178508511, Verbindung

HRID 1707481
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1707481
C1(C([O:14][C:15]([C:17]2[N:22]3[C:23](=[O:73])[C@@H:24]([NH:25][C:26](=[O:72])/[C:27](/[C:47]4[N:48]=[C:49]([NH:52]C(C5C=CC=CC=5)(C5C=CC=CC=5)C5C=CC=CC=5)[S:50][CH:51]=4)=[N:28]\[O:29][CH2:30][C:31]([O:33]C(C4C=CC=CC=4)C4C=CC=CC=4)=[O:32])[C@H:21]3[S:20][CH2:19][C:18]=2[S:74][CH:75](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[S:76][C:77]2[N:78]=[N:79][NH:80][CH:81]=2)=[O:16])C2C=CC=CC=2)C=CC=CC=1.[Cl-].[Al+3].[Cl-].[Cl-].C(=O)([O-])O.[Na+:109]>C(O)=O.O.C1(OC)C=CC=CC=1.Cl>[Na+:109].[NH2:52][C:49]1[S:50][CH:51]=[C:47](/[C:27](=[N:28]/[O:29][CH2:30][C:31]([O:33][Na:109])=[O:32])/[C:26]([NH:25][C@@H:24]2[C:23](=[O:73])[N:22]3[C:17]([C:15]([O-:14])=[O:16])=[C:18]([S:74][CH2:75][S:76][C:77]4[N:78]=[N:79][NH:80][CH:81]=4)[CH2:19][S:20][C@H:21]23)=[O:72])[N:48]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 516892Sodium BicarbonateHCID 6451240Aluminum(III) ChlorideHCID 88301232benzhydryl (6R,7R)-7-[[(2Z)-2-(2-benzhydryloxy-2-oxoethoxy)imino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-8-oxo-3-[2,2,2-triphenyl-1-(1H-triazol-4-ylsulfanyl)ethyl]sulfanyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

Produkt 1

HCID 178508511HCID 178508511, Verbindung
Ausbeute 26 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 284Formic AcidLösungsmittelHCID 313Hydrochloric AcidLösungsmittelHCID 962WaterLösungsmittel2×HCID 7519AnisoleLösungsmittel

Versuchsvorschrift

A solution of 7β-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-(diphenylmethoxycarbonylmethoxyimino)acetamido]-3-(trityl-1,2,3-triazol-4-ylthio-methylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (1.04 g: 0.749 mMol.) in a mixture of 98% formic acid (16 ml) and water (0.8 ml) is stirred at room temperature for 3 hours. The reaction mixture is concentrated. The residue is washed with ether, filtered, end dried. To a solution of this residue in a mixture of anisole (2 ml) and nitro- methane (8 ml) at -40° C. is added a solution of aluminum chloride (0.50 g: 3.76 mMol.) in anisole (2 ml), and the mixture is stirred at -30° to -40° C. for 1 hour. The reaction mixture is diluted with 1N-hydrochloric acid (3.8 ml) and water, washed with ethyl acetate, and concentrated under reduced pressure to remove organic solvents. The remaining aqueous solution is subjected to chromatography over styrene-divinyl-benzene copolymer (methanol: water=4:1). The residue is washed with ethyl acetate and resulting powder is dissolved in dilute aqueous sodium hydrogen carbonate, and purified by chromatography over analytical styrene-divinylbenzene (water). The eluate is lyophilized and pulverized with ethyl acetate to give 7β-[(Z)-2-(2-aminothiazol-4-yl)-2-(sodiooxycarbonylmethoxyimino)acetamido]-3-(1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid sodium salt (121 mg) as pale yellow white powder. Yield: 26%.

Aufarbeitung

  1. concentrationThe reaction mixture is concentrated
  2. washThe residue is washed with ether
  3. filtrationfiltered
  4. customend dried
  5. additionTo a solution of this residue in a mixture of anisole (2 ml) and nitro- methane (8 ml) at -40° C.
  6. stirringthe mixture is stirred at -30° to -40° C. for 1 hour
  7. washwashed with ethyl acetate
  8. concentrationconcentrated under reduced pressure
  9. customto remove organic solvents
  10. washThe residue is washed with ethyl acetate
  11. customresulting powder
  12. custompurified by chromatography over analytical styrene-divinylbenzene (water)

Quellen und Nachweise

ORD-Eintrag
ord-93d1996081b74d3283a160aa9eda0f0d
Quelldatensatz
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05352792

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