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Formic Acid → HCID 178502832, compound

HRID 483026
Notes
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Reaction equation

HRID 483026 reaction equation
[CH:1]([OH:3])=[O:2].C([NH:23][C:24]1[S:25][CH:26]=[C:27](/[C:29](=[N:53]/[O:54][CH3:55])/[C:30]([NH:32][C@@H:33]2[C:51](=[O:52])[N:35]3[C:36]([C:48]([OH:50])=[O:49])=[C:37]([CH2:40][S:41][C:42]4[N:46]([NH2:47])[N:45]=[N:44][N:43]=4)[CH2:38][S:39][C@H:34]23)=[O:31])[N:28]=1)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>O>[CH:1]([OH:3])=[O:2].[NH2:23][C:24]1[S:25][CH:26]=[C:27](/[C:29](=[N:53]/[O:54][CH3:55])/[C:30]([NH:32][C@@H:33]2[C:51](=[O:52])[N:35]3[C:36]([C:48]([OH:50])=[O:49])=[C:37]([CH2:40][S:41][C:42]4[N:46]([NH2:47])[N:45]=[N:44][N:43]=4)[CH2:38][S:39][C@H:34]23)=[O:31])[N:28]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 284Formic AcidHCID 178502831(6R,7R)-3-[(1-aminotetrazol-5-yl)sulfanylmethyl]-7-[[(2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Product 1

HCID 178502832HCID 178502832, compoundYield 93.9%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To 80% formic acid (17 ml) was added 7β-[2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-[(1-amino-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid (4.3 g, 5.7 mmol) with stirring at room temperature and the mixture was stirred for an hour and a quarter. After adding water (85 ml), the mixture was filtered to remove insoluble material and the filtrate was concentrated below 45° C. The residue was treated with tetrahydrofuran (10 ml)-ether (5 ml) and concentrated again under reduced pressure. The residue was treated with ether to give pale yellow substances of 7β-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-[(1-amino-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid formate (2.98 g, 93.9%).

Workup

  1. stirringthe mixture was stirred for an hour
  2. filtrationthe mixture was filtered
  3. customto remove insoluble material
  4. concentrationthe filtrate was concentrated below 45° C
  5. additionThe residue was treated with tetrahydrofuran (10 ml)-ether (5 ml)
  6. concentrationconcentrated again under reduced pressure
  7. additionThe residue was treated with ether

Sources & evidence

ORD record
ord-a0001485d4524b978b47addae3345c0b
Source dataset
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04576938

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes