Water → Trisodium 3-acetoxymethyl-7beta-(2-carboxy-2-phenylacetamido)-3-cephem-4-phosphonate

HRID 26586Notes

Reaction equation

HRID 26586 reaction equation
[C:1]([O:4][CH2:5][C:6]1[CH2:7][S:8][C@@H:9]2[C@H:17]([NH:18][C:19](=[O:43])[CH:20]([C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)[C:21]([O:23]C(C3C=CC=CC=3)C3C=CC=CC=3)=[O:22])[C:16](=[O:44])[N:10]2[C:11]=1[P:12]([OH:15])(=[O:14])[OH:13])(=[O:3])[CH3:2].C1(OC)C=CC=CC=1.FC(F)(F)C(O)=O.O.C([O-])(O)=O.[Na+:65]>C(Cl)Cl>[C:1]([O:4][CH2:5][C:6]1[CH2:7][S:8][C@@H:9]2[C@H:17]([NH:18][C:19](=[O:43])[CH:20]([C:21]([OH:23])=[O:22])[C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)[C:16](=[O:44])[N:10]2[C:11]=1[P:12]([O-:15])(=[O:13])[O-:14])(=[O:3])[CH3:2].[Na+:65].[Na+:65].[Na+:65]

Participants

7

Procedure

One gram of 3-acetoxymethyl-7β-(2-phenyl-2-benzhydryloxycarbonylacetamido)-3-cephem-4-phosphonic acid is dissolved in 2 ml. anisole and treated for two minutes at 0° with 10 ml. trifluoroacetic acid. The mixture is pumped at 0.1 mm at 25° until most of the anisole is removed, and then more anisole is added and pumped off to insure complete removal of TFA. The residue is taken up in 100 ml. water containing three equivalents of NaHCO3, washed with methylene chloride and lyophilized, affording the product, trisodium 3-acetoxymethyl-7β-(2-carboxy-2-phenylacetamido)-3-cephem-4-phosphonate.

Workup

  1. customis pumped at 0.1 mm at 25°
  2. customis removed
  3. additionmore anisole is added
  4. customremoval of TFA

Sources & evidence

ORD record
ord-9a7e64c21a794da1bb823a937f6e27c3
Source dataset
uspto-grants-1979_04
Patent number
US04150223

Reaction notes

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