Trifluoroacetic acid → HCID 131712318, compound

HRID 1758390Notes

Reaction equation

HRID 1758390 reaction equation
FC(F)(F)C(O)=O.[CH:8]([NH:10][C:11]1[S:12][CH:13]=[C:14]([C:16](=[N:42][O:43][CH2:44][C:45]([O:47]C(C)(C)C)=[O:46])[C:17]([NH:19][CH:20]2[C:40](=[O:41])[N:22]3[C:23]([C:27]([O:29][CH2:30][C:31]4[CH:36]=[CH:35][C:34]([N+:37]([O-:39])=[O:38])=[CH:33][CH:32]=4)=[O:28])=[CH:24][CH2:25][S:26][C@H:21]23)=[O:18])[N:15]=1)=[O:9]>C1(OC)C=CC=CC=1>[CH:8]([NH:10][C:11]1[S:12][CH:13]=[C:14]([C:16](=[N:42][O:43][CH2:44][C:45]([OH:47])=[O:46])[C:17]([NH:19][CH:20]2[C:40](=[O:41])[N:22]3[C:23]([C:27]([O:29][CH2:30][C:31]4[CH:32]=[CH:33][C:34]([N+:37]([O-:39])=[O:38])=[CH:35][CH:36]=4)=[O:28])=[CH:24][CH2:25][S:26][C@H:21]23)=[O:18])[N:15]=1)=[O:9]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 131712317HCID 131712317, compound

Product 1

HCID 131712318HCID 131712318, compoundYield 89.8%

Reagents, catalysts & solvents 1

HCID 7519AnisoleSolvent

Procedure

Trifluoroacetic acid (40 ml.) was added to a suspension of 4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-t-butoxycarbonylmethoxyiminoacetamido]-3-cephem-4-carboxylate (syn isomer, 10 g.) in anisole (10 ml.) at 5° C., and stirred at room temperature for 70 minutes. After evaporating the solvent from the resultant mixture in vacuo, the residue was triturated with diethyl ether. The precipitates were collected by filtration and dried to give 4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-cephem-4-carboxylate (syn isomer, 8.2 g.).

Workup

  1. customAfter evaporating the solvent from the resultant mixture in vacuo
  2. customthe residue was triturated with diethyl ether
  3. filtrationThe precipitates were collected by filtration
  4. customdried

Sources & evidence

ORD record
ord-ff20038d29ae4c76a5d780b49e68c3ba
Source dataset
uspto-grants-1983_02
Patent number
US04372952

Reaction notes

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