HCID 131712246, compound → HCID 131712245, compound

HRID 2287006Notes

Reaction equation

HRID 2287006 reaction equation
[CH3:1][O:2][N:3]=[C:4]([C:37]1[N:41]=[C:40]([NH2:42])[S:39][N:38]=1)[C:5]([NH:7][CH:8]1[C:35](=[O:36])[N:10]2[C:11]([C:32]([OH:34])=[O:33])=[C:12]([CH2:15][S:16][C:17]3[N:21]([CH2:22][CH2:23][NH:24]C(OC(C)(C)C)=O)[N:20]=[N:19][N:18]=3)[CH2:13][S:14][C@H:9]12)=[O:6]>C(O)=O>[CH3:1][O:2][N:3]=[C:4]([C:37]1[N:41]=[C:40]([NH2:42])[S:39][N:38]=1)[C:5]([NH:7][CH:8]1[C:35](=[O:36])[N:10]2[C:11]([C:32]([OH:34])=[O:33])=[C:12]([CH2:15][S:16][C:17]3[N:21]([CH2:22][CH2:23][NH2:24])[N:20]=[N:19][N:18]=3)[CH2:13][S:14][C@H:9]12)=[O:6]

Participants

3

Procedure

A solution of 7-[2-methoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-[1-{2-(N-t-butoxycarbonylamino)ethyl}-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (2.0 g) in 99% formic acid (20 ml) was stirred for 2.5 hours at ambient temperature. The mixture was evaporated to dryness and the residue was dissolved in an aqueous solution of sodium bicarbonate and adjusted to pH 3 with 10% hydrochloric acid. A resulting precipitate was filtered off and the filtrate was subjected to column chromatography on non ion adsorption resin (Diaion HP 20) (Trademark: prepared by Mitsubishi Chemical Industries). The column was washed with water and eluted with 50% aqueous methanol. The eluate was evaporated to remove methanol and then lyophilized to give 7-[2-methoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-[1-(2-aminoethyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (250 mg). mp 200° to 205° C. (dec.)

Workup

  1. customThe mixture was evaporated to dryness
  2. dissolutionthe residue was dissolved in an aqueous solution of sodium bicarbonate
  3. filtrationA resulting precipitate was filtered off
  4. customthe filtrate was subjected to column chromatography on non ion adsorption resin (Diaion HP 20) (Trademark: prepared by Mitsubishi Chemical Industries)
  5. washThe column was washed with water
  6. washeluted with 50% aqueous methanol
  7. customThe eluate was evaporated
  8. customto remove methanol

Sources & evidence

ORD record
ord-083f1707cfa5492da4bd71bf2c76a53e
Source dataset
uspto-grants-1981_05
Patent number
US04268509

Reaction notes

Loading…