Pyridine → Diphenylmethyl 3-methoxyiminomethyl-7-amino-3-cephem-4-carboxylate

HRID 1287994Notes

Reaction equation

HRID 1287994 reaction equation
[CH3:1][O:2][N:3]=[CH:4][C:5]1[CH2:6][S:7][C@@H:8]2[CH:28]([NH:29]C(=O)CC3SC=CC=3)[C:27](=[O:38])[N:9]2[C:10]=1[C:11]([O:13][CH:14]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12].N1C=CC=CC=1.P(Cl)(Cl)(Cl)(Cl)Cl>C1C=CC=CC=1.CO.O>[CH3:1][O:2][N:3]=[CH:4][C:5]1[CH2:6][S:7][C@@H:8]2[CH:28]([NH2:29])[C:27](=[O:38])[N:9]2[C:10]=1[C:11]([O:13][CH:14]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:12]

Participants

7

Procedure

To a solution of diphenylmethyl 3-methoxyiminomethyl- 7-(2-thienylacetamido)-3 -cephem-4-carboxylate (887 mg) in benzene (48 ml) are added pyridine (0.26 ml) and phosphorous pentachloride (676 mg) in benzene (48 ml), and the mixture is stirred for 90 minutes. The mixture is diluted with methanol (96 ml), stirred for 2.5 hours, diluted with water (9.6 ml), stirred for 20 minutes, and evaporated at a temperature lower than 40° C. The residue is dissolved in ethyl acetate, washed with water, aqueous sodium hydrogen carbonate and water, dried and evaporated. The residue crystallizes from a mixture of ether and petroleum ether to give diphenylmethyl 3-methoxyiminomethyl-7 -amino-3 -cephem-4-carboxylate (639 mg; 94.2%). m.p. 135°-145° C.

Workup

  1. stirringstirred for 2.5 hours
  2. stirringstirred for 20 minutes
  3. customevaporated at a temperature lower than 40° C
  4. dissolutionThe residue is dissolved in ethyl acetate
  5. washwashed with water, aqueous sodium hydrogen carbonate and water
  6. customdried
  7. customevaporated
  8. customThe residue crystallizes from a mixture of ether and petroleum ether

Sources & evidence

ORD record
ord-db7103ec61d54d58a4832ef09703859c
Source dataset
uspto-grants-1976_10
Patent number
US03987039

Reaction notes

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