p-Toluenesulfonic acid → Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate

HRID 905420Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 905420
C1(N[CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)CCCCC1.[CH:14](=[N:22][CH:23]1[C:35](=[O:36])[N:25]2[C:26]([C:32]([OH:34])=[O:33])=[C:27]([CH2:30][OH:31])[CH2:28][S:29][C@H:24]12)[C:15]1[C:16](=[CH:18][CH:19]=[CH:20][CH:21]=1)[OH:17].[C:37]1([CH3:47])[CH:42]=[CH:41][C:40](S(O)(=O)=O)=[CH:39][CH:38]=1>C(OCC)(=O)C>[CH:14](=[N:22][CH:23]1[C:35](=[O:36])[N:25]2[C:26]([C:32]([O:34][CH:47]([C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)=[O:33])=[C:27]([CH2:30][OH:31])[CH2:28][S:29][C@H:24]12)[C:15]1[C:16](=[CH:18][CH:19]=[CH:20][CH:21]=1)[OH:17]

Komponenten

4

Versuchsvorschrift

To a suspension of 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylic acid dicyclohexylamine salt (3 g) in ethyl acetate (60 ml) was added dropwise an ethyl acetate solution of p-toluenesulfonic acid (1.1 g) with stirring, and the reaction mixture was stirred for an hour at ambient temperature. After the precipitate was filtered off, the filtrate was treated with a solution of excess diphenyldiazomethane in ethyl acetate for an hour. The solvent was distilled off, and the residue was pulverized with diisopropyl ether, collected by filtration and dried to give benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate (2.66 g).

Aufarbeitung

  1. stirringthe reaction mixture was stirred for an hour at ambient temperature
  2. filtrationAfter the precipitate was filtered off
  3. additionthe filtrate was treated with a solution of excess diphenyldiazomethane in ethyl acetate for an hour
  4. distillationThe solvent was distilled off
  5. filtrationcollected by filtration
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8cb93efd4eaf4a50a25b783014da18a2
Quelldatensatz
uspto-grants-1983_12
Patentnummer
US04423213

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