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Hydrochloric Acid → HCID 178502825, compound

HRID 490018
Notes
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Reaction equation

HRID 490018 reaction equation
[NH2:1][C@H:2]([C:10]([OH:12])=[O:11])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:9])[NH2:8].[CH3:13][N:14]1[N:20]=[C:19]([OH:21])[C:17](=[O:18])[N:16]=[C:15]1[S:22][CH2:23][C:24]1[CH2:45][S:44][C@@H:27]2[C@H:28]([NH:31][C:32](/[C:34](/[C:38]3[N:42]=[C:41]([NH2:43])[S:40][CH:39]=3)=[N:35]\[O:36][CH3:37])=[O:33])[C:29](=[O:30])[N:26]2[C:25]=1[C:46]([OH:48])=[O:47].Cl>O>[CH3:13][N:14]1[N:20]=[C:19]([OH:21])[C:17](=[O:18])[N:16]=[C:15]1[S:22][CH2:23][C:24]1[CH2:45][S:44][C@@H:27]2[C@H:28]([NH:31][C:32](/[C:34](/[C:38]3[N:42]=[C:41]([NH2:43])[S:40][CH:39]=3)=[N:35]\[O:36][CH3:37])=[O:33])[C:29](=[O:30])[N:26]2[C:25]=1[C:46]([OH:48])=[O:47].[NH2:1][C@H:2]([C:10]([OH:12])=[O:11])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:8])[NH2:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 178418600HCID 178418600, compound3×HCID 178502822HCID 178502822, compound2×

Product 1

HCID 178502825HCID 178502825, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Procedure

About 582 mg (3.34 mole) of arginine was dissolved in 50 ml of distilled water. Additionally, about 1.0 grams (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 pH reached 6.0. The ceftriaxone solution was then added to the arginine solution and mixed by a magnetic stirrer at room temperature for 1 hour forming a ceftriaxone-arginine solution. To the ceftriaxone-arginine solution was added about 400 mg of carrageenan and the solution was mixed by magnetic stirrer at room temperature for 2 hours. A ceftriaxone-arginine-carrageenan complex was formed which was freeze-dried while in the swollen state, yielding about 1.84 g of the freeze dried complex.

Workup

  1. additionmixed by a magnetic stirrer at room temperature for 1 hour

Sources & evidence

ORD record
ord-19e12ca503e54b8096b410129fa742eb
Source dataset
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07527807B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes