Acetic Acid → HCID 70591997, compound

HRID 1395509Notes

Reaction equation

HRID 1395509 reaction equation
[CH3:1][N:2]1[C:6]([S:7][CH2:8][C:9]2([CH3:41])[CH:13]([C:14]([O:16]CC(Cl)(Cl)Cl)=[O:15])[N:12]3[C:22](=[O:40])[CH:23]([NH:24][C:25]([C:27]4[C:28]([C:33]5[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=5[Cl:39])=[N:29][O:30][C:31]=4[CH3:32])=[O:26])[C@H:11]3[S:10]2)=[N:5][N:4]=[N:3]1.[C:42](O)(=O)[CH3:43]>CN(C)C=O.[Zn]>[CH3:1][N:2]1[C:6]([S:7][CH2:8][C:9]2([CH3:41])[CH:13]([C:14]([OH:16])=[O:15])[N:12]3[C:22](=[O:40])[CH:23]([NH:24][C:25]([C:27]4[C:28]([C:33]5[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=5[Cl:39])=[N:29][O:30][C:31]=4[CH3:32])=[O:26])[C@H:11]3[S:10]2)=[N:5][N:4]=[N:3]1.[CH2:28]([NH:29][CH2:42][CH2:43][NH:29][CH2:28][C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1

Participants

5

Conditions

Temperature
-15 °C

Procedure

2,2,2-Trichloroethyl 2-(1-methyl-1H-tetrazol-5-yl)thiomethyl-2-methyl-6-[3-(2-chlorophenyl)-5-methylisoxazole-4-carboxamido]penam-3-carboxylate (0.67 g) was dissolved in dimethylformamide (5 ml). To this solution were added acetic acid (0.8 ml) and zinc powder (0.7 g) under cooling at -15° C. and the mixture was stirred for 2 hours at the same temperature. After the reaction, zinc powder was filtered off and the filtrate was poured into 5% hydrochloric acid (20 ml) and then extraxted with ethyl acetate. The extract was washed with water, dried and the solvent was distilled off. The residue was dissolved in methanol (0.8 ml) and to this solution was added a solution of N,N'-dibenzylethylenediamine diacetate (0.18 g) in water (5 ml) and precipitates were collected by filtration, washed with water and dried to give N,N'-dibenzylethylenediamine 2-(1-methyl-1H-tetrazol-5-yl)thiomethyl-2-methyl-6-[3-(2-chlorophenyl)-5-methylisoxazole-4-carboxamido]penam-3-carboxylate (0.24 g), mp. 117° to 119° C. (dec.).

Workup

  1. filtrationwas filtered off
  2. additionthe filtrate was poured into 5% hydrochloric acid (20 ml)
  3. washThe extract was washed with water
  4. customdried
  5. distillationthe solvent was distilled off
  6. dissolutionThe residue was dissolved in methanol (0.8 ml) and to this solution
  7. additionwas added a solution of N,N'-dibenzylethylenediamine diacetate (0.18 g) in water (5 ml)
  8. customprecipitates
  9. filtrationwere collected by filtration
  10. washwashed with water
  11. customdried

Sources & evidence

ORD record
ord-62b007fcdcab401c9f5a552354cee69b
Source dataset
uspto-grants-1980_05
Patent number
US04203897

Reaction notes

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