Triethylamine → 1175-97-9

HRID 1606435Notes

Reaction equation

HRID 1606435 reaction equation
[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([OH:23])=[O:22].O.O.O.S([O-])([O-])(=O)=O.[Mg+2].[CH2:34]([N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])[CH3:35]>ClCCl>[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([OH:23])=[O:22].[CH2:34]([N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])[CH3:35]

Participants

5

Procedure

By treating a mixture of 806 mg. of ampicillin trihydrate, 600 mg. of magnesium sulfate, 0.42 ml. of triethylamine, and 15 ml. of dichloromethane as in Example 63, a dichloromethane solution of ampicillin triethylamine salt was obtained.

Workup

  1. additionBy treating
  2. additiona mixture of 806 mg

Sources & evidence

ORD record
ord-c8d98ae11ae642a5aeb636fd9b93467b
Source dataset
uspto-grants-1976_04
Patent number
US03953428

Reaction notes

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