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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
ノート
印刷プレビュー

反応式

HRID 1873343 の反応式
[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]
参加物実験手順出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 5962L-Lysine2 回HCID 178418600HCID 178418600、化合物HCID 178502822HCID 178502822、化合物HCID 178502825HCID 178502825、化合物

生成物 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

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

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.

出典と根拠

ORDレコード
ord-83e2860a1c0941d3a6e18ab365509ab4
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08303989B2

反応ノート

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