N,N-Diethylaniline → HCID 178468136, compound

HRID 1449200Notes

Reaction equation

HRID 1449200 reaction equation
C([O:5][C:6]([C:8]1[N:13]2[C:14](=[O:19])[C@:15]([NH2:18])([O:16][CH3:17])[C@H:12]2[S:11][CH2:10][C:9]=1[C:20]([CH2:30][PH:31]([O:33]C(C)(C)C)=[O:32])([S:24][C:25]1[NH:29][N:28]=[N:27][N:26]=1)[O:21][CH2:22][CH3:23])=[O:7])(C)(C)C.C(N(CC)[C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1)C>C(Cl)Cl>[C:15]([NH:18][C@:15]1([O:16][CH3:17])[C:14](=[O:19])[N:13]2[C:8]([C:6]([OH:5])=[O:7])=[C:9]([C:20]([CH2:30][PH:31]([OH:33])=[O:32])([S:24][C:25]3[NH:26][N:27]=[N:28][N:29]=3)[O:21][CH2:22][CH3:23])[CH2:10][S:11][C@H:12]12)(=[O:16])[C@@H:14]([C:41]1[CH:42]=[CH:43][CH:44]=[CH:45][CH:46]=1)[OH:19]

Participants

4

Reactant 2

HCID 7061N,N-DiethylanilineHCID 178468128HCID 178468128, compound

Product 1

HCID 178468136HCID 178468136, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

A solution of 1.16 g (2 mmol) of 7β-amino-7α-methoxy-3-(1-ethoxy-t-butoxyphosphinylmethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid t-butyl ester and 0.30 g (2 mmol) of N,N-diethylaniline in 100 ml of dry methylene chloride is stirred at 0°-5° while 0.56 g (2 mmol) of D-O-dichloroacetylmandeloyl chloride in 10 ml of methylene chloride is added dropwise over 10 minutes. The mixture is stirred in the cold for 30 minutes then warmed to room temperature and stirred for an additional 30 minutes. The solution is washed with 50 ml of cold dilute hydrochloric acid and 50 ml of cold 5% aqueous sodium bicarbonate, dried and evaporated to dryness. The residue is dissolved in a mixture of 10 ml of trifluoroacetic acid and 2 ml of m-dimethoxybenzene and stirred at ambient temperature for 2 hours. The excess trifluoroacetic acid is evaporated under vacuum and the residue is partitioned between 50 ml of ether and 50 ml of water and adjusted to pH 9.3-9.5 with 5% aqueous sodium carbonate. The organic phase is separated and discarded. The aqueous phase is stirred at pH 9.3-9.5 for 30 minutes, layered with ethyl acetate and adjusted to pH 3.0 with dilute hydrochloric acid. After separation of the layers, the aqueous phase is adjusted to pH 7 with sodium bicarbonate and passed through a XAD-7 resin column. The product-containing fractions are combined, stirred with Amberlite IR-120H ion-exchange resin and lyophilized to give the title compound.

Workup

  1. additionis added dropwise over 10 minutes
  2. stirringstirred for an additional 30 minutes
  3. washThe solution is washed with 50 ml of cold dilute hydrochloric acid and 50 ml of cold 5% aqueous sodium bicarbonate
  4. customdried
  5. customevaporated to dryness
  6. dissolutionThe residue is dissolved in a mixture of 10 ml of trifluoroacetic acid and 2 ml of m-dimethoxybenzene
  7. stirringstirred at ambient temperature for 2 hours
  8. customThe excess trifluoroacetic acid is evaporated under vacuum
  9. customthe residue is partitioned between 50 ml of ether and 50 ml of water
  10. customThe organic phase is separated
  11. stirringThe aqueous phase is stirred at pH 9.3-9.5 for 30 minutes
  12. customAfter separation of the layers
  13. stirringstirred with Amberlite IR-120H ion-exchange resin

Sources & evidence

ORD record
ord-47ccdfc3d4be4d3bb6c16006740a8e8f
Source dataset
uspto-grants-1980_02
Patent number
US04189573

Reaction notes

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