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

HRID 1199762Notes

Reaction equation

HRID 1199762 reaction equation
[N+](C)([O-])=O.C[C:6]([O:8][CH2:9][C:10]1[CH2:19][S:18][C@@H:13]2[C@H:14]([NH2:17])[C:15](=[O:16])[N:12]2[C:11]=1[C:20]([OH:22])=[O:21])=O.N>[Br-].[Zn+2].[Br-].CO.O>[NH2:17][CH:14]1[C:15](=[O:16])[N:12]2[C:11]([C:20]([OH:22])=[O:21])=[C:10]([CH2:9][O:8][CH3:6])[CH2:19][S:18][C@H:13]12

Participants

7

Conditions

Temperature
60 °C

Procedure

To 10 ml of nitromethane were added 2.72 g of 7-ACA, 8 g of zinc bromide and 0.9 g of methanol. The mixture was heated at 60° C. for 80 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture were added 10 ml of water and 5 ml of methanol. Then, the mixture was adjusted to pH 7.5 with aqueous ammonia at a temperature of from 0° C. to 5° C. The resulting precipitate was filtered off, and then washed with water. The filtrate was combined with the washings. The resulting mixture was adjusted to pH 3.5 with 36 % hydrochloric acid to thereby form a precipitate. The precipitate was collected by filtration, and washed with 10 ml of cold water and, then, with 10 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 0.71 g. The yield of the desired product was 29 %.

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. customto thereby form a precipitate
  7. filtrationThe precipitate was collected by filtration
  8. washwashed with 10 ml of cold water

Sources & evidence

ORD record
ord-ac75637d49434fed9694c62a8231594c
Source dataset
uspto-grants-1990_02
Patent number
US04902793

Reaction notes

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