Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid

HRID 1199770Notes

Reaction equation

HRID 1199770 reaction equation
C(Cl)(Cl)(Cl)Cl.C[C:7]([O:9][CH2:10][C:11]1[CH2:20][S:19][C@@H:14]2[C@H:15]([NH2:18])[C:16](=[O:17])[N:13]2[C:12]=1[C:21]([OH:23])=[O:22])=O.[B].N>O.CO>[NH2:18][CH:15]1[C:16](=[O:17])[N:13]2[C:12]([C:21]([OH:23])=[O:22])=[C:11]([CH2:10][O:9][CH3:7])[CH2:20][S:19][C@H:14]12

Participants

7

Conditions

Temperature
60 °C

Procedure

To 10 ml of carbon tetrachloride were added 2.72 g of 7-ACA, 4.3 g of a boron trifluoridediethylether complex, and 3.5 g of methanol. The mixture was heated at 60° C. for 35 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture was added 20 ml of cold water. Then, the mixture was adjusted to pH 7.5 with 28% aqueous ammonia at a temperature of 5° C. The resulting precipitate was filtered off, and then washed with water. The filtrate was combined with the washings. The resulting mixture was applied to the same column as used in Example 2. The elution was conducted using water as an eluent. The resulting eluate was adjusted to pH 3.5 with 36% hydrochloric acid to hereby form a precipitate. The precipitate was collected by filtration, and washed with 5 ml of cold water and, then, with 5 ml of cold methanol to obtain the desired product, namely 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. The amount of the desired product was 0.27 g. The yield of the desired product was as low as 11.1%.

Workup

  1. customa reaction
  2. customAfter completion of the reaction
  3. temperaturethe reaction mixture was cooled to 5° C
  4. filtrationThe resulting precipitate was filtered off
  5. washwashed with water
  6. washThe elution
  7. customto hereby form a precipitate
  8. filtrationThe precipitate was collected by filtration
  9. washwashed with 5 ml of cold water

Sources & evidence

ORD record
ord-c5e69752229945e28614de60d58b7371
Source dataset
uspto-grants-1990_02
Patent number
US04902793

Reaction notes

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