Bicarbonate Ion → (6R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(methanehydrazonoylhydrazinylidene)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

HRID 1860469

반응식

HRID 1860469 반응식
C(=O)([O-])O.[C:5]([NH2:9])(N)=[N:6][NH2:7].FC(F)(F)C([O-])=O.O[CH:18]1[C:26]2[CH2:25][S:24][CH:23]3[CH:27]([NH:30][C:31](=[O:42])/[C:32](/[C:36]4[N:37]=[C:38]([NH2:41])[S:39][CH:40]=4)=[N:33]\[O:34][CH3:35])[C:28](=[O:29])[N:22]3[C:21]=2[C:20](=[O:43])[O:19]1.C(#[N:46])C>Cl>[NH2:41][C:38]1[S:39][CH:40]=[C:36](/[C:32](=[N:33]/[O:34][CH3:35])/[C:31]([NH:30][CH:27]2[C:28](=[O:29])[N:22]3[C:21]([C:20]([OH:19])=[O:43])=[C:26]([CH:18]=[N:46][NH:9][CH:5]=[N:6][NH2:7])[CH2:25][S:24][C@H:23]23)=[O:42])[N:37]=1

참가 물질

7

실험 절차

1.24 g of the hydrogen carbonate of aminoguanidine are dissolved in 9.15 ml of 2 N HCl and added under stirring to a solution of 3.2 g of the trifluoroacetate of N-(1,4,5a,6-tetrahydro-3-hydroxy-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]-thiazin-6-yl)-2-(2-aminothiazol-4yl)-(Z)-2-methoxyimino acetic acid amide in 125 ml of 4% aqueous acetonitrile. After ca. 90 minutes the precipitated dihydrochloride of 7-[(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino-3-[[(aminoimino-methyl)-hydrazono]methyl]-3-cephem-4-carboxylic acid is filtered off, washed with acetonitrile and dried.

후처리

  1. additionadded
  2. filtrationAfter ca. 90 minutes the precipitated dihydrochloride of 7-[(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino-3-[[(aminoimino-methyl)-hydrazono]methyl]-3-cephem-4-carboxylic acid is filtered off
  3. washwashed with acetonitrile
  4. customdried

출처 및 근거

ORD 기록
ord-c359d1bafce448be91baa3d2504fd3e8
출처 데이터셋
uspto-grants-2003_03
특허 번호
US06531465B1

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