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Hydrochloric Acid → (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-5,6-dioxo-1H-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;(2S)-2,6-diaminohexanoic acid

HRID 1873343
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1873343
[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7].[CH3:11][N:12]1[N:18]=[C:17]([OH:19])[C:15](=[O:16])[N:14]=[C:13]1[S:20][CH2:21][C:22]1[CH2:43][S:42][C@@H:25]2[C@H:26]([NH:29][C:30](/[C:32](/[C:36]3[N:40]=[C:39]([NH2:41])[S:38][CH:37]=3)=[N:33]\[O:34][CH3:35])=[O:31])[C:27](=[O:28])[N:24]2[C:23]=1[C:44]([OH:46])=[O:45].N[C@H](C(O)=O)CCCNC(=N)N.Cl.CN1N=C(O)C(=O)N=C1SCC1CS[C@@H]2[C@H](NC(/C(/C3N=C(N)SC=3)=N\OC)=O)C(=O)N2C=1C(O)=O.N[C@H](C(O)=O)CCCNC(=N)N>O>[CH3:11][N:12]1[N:18]=[C:17]([OH:19])[C:15](=[O:16])[N:14]=[C:13]1[S:20][CH2:21][C:22]1[CH2:43][S:42][C@@H:25]2[C@H:26]([NH:29][C:30](/[C:32](/[C:36]3[N:40]=[C:39]([NH2:41])[S:38][CH:37]=3)=[N:33]\[O:34][CH3:35])=[O:31])[C:27](=[O:28])[N:24]2[C:23]=1[C:44]([OH:46])=[O:45].[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7]
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Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 5962L-Lysine2×HCID 178418600HCID 178418600, VerbindungHCID 178502822HCID 178502822, VerbindungHCID 178502825HCID 178502825, Verbindung

Produkt 1

HCID 178502824
(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-5,6-dioxo-1H-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;(2S)-2,6-diaminohexanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Versuchsvorschrift

About 610 mg (3.34 mole) of lysine was dissolved in 50 ml of distilled water. Additionally, 1.0 gram (1.67 mole) of ceftriaxone was dissolved in 50 ml of a separate volume of distilled water. The solution containing arginine was adjusted with 1N—HCl until the solution reached pH 6.0. The ceftriaxone solution was then added to the lysine solution and stirred by a magnetic stirrer at room temperature for 1 hour forming a ceftriaxone-lysine solution. To the ceftriaxone-lysine solution was added about 400 mg of carrageenan and the solution was stirred by magnetic stirrer at room temperature for 2 hours. A ceftriaxone-lysine-carrageenan hydrogel was formed. The hydrogel was then freeze-dried while in the swollen state, yielding about 1.92 g of the freeze-dried complex.

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ORD-Eintrag
ord-83e2860a1c0941d3a6e18ab365509ab4
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08303989B2

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