Hydrochloric Acid → HCID 88724528, compound

HRID 1706535Notes

Reaction equation

HRID 1706535 reaction equation
[C:1]([O:5][C:6]([NH:8][CH:9]([C:49]([OH:51])=[O:50])[CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]([C:45](=[O:48])[CH:46]=[O:47])[CH:20]2[CH2:23][N:22]([CH:24]([C:28]3[CH:33]=[CH:32][C:31]([O:34][C:35](=[O:43])[NH:36]C(=O)C(Cl)(Cl)Cl)=[CH:30][CH:29]=3)[C:25]([OH:27])=[O:26])[C:21]2=[O:44])=[CH:15][CH:14]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(=O)(O)[O-].[Na+].CO.Cl>O>[C:1]([O:5][C:6]([NH:8][CH:9]([C:49]([OH:51])=[O:50])[CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]([C:45](=[O:48])[CH:46]=[O:47])[CH:20]2[CH2:23][N:22]([CH:24]([C:28]3[CH:29]=[CH:30][C:31]([O:34][C:35](=[O:43])[NH2:36])=[CH:32][CH:33]=3)[C:25]([OH:27])=[O:26])[C:21]2=[O:44])=[CH:15][CH:14]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

6

Procedure

2-[3-{4-(3-tert-Butoxycarbonylamino-3-carboxypropoxy)phenylglyoxyloylamino}-2-oxo-1-azetidinyl]-2-[4-{N-(2,2,2-trichloroacetyl)carbamoyloxy}phenyl]acetic acid (550 mg.) was suspended in water (5 ml.), and to the suspension there were added sodium bicarbonate (250 mg.) and methanol (1 ml.). The mixture was stirred at ambient temperature for 7 hours. The reaction mixture was adjusted to pH 2 with dilute hydrochloric acid and the precipitating material was collected by filtration. The material was washed with water and then dried to give 2-[3-{4-(3-tert-butoxycarbonylamino-3-carboxypropoxy)phenylglyoxyloylamino}-2-oxo-1-azetidinyl]-2-(4-carbamoyloxyphenyl)acetic acid.

Workup

  1. filtrationthe precipitating material was collected by filtration
  2. washThe material was washed with water
  3. customdried

Sources & evidence

ORD record
ord-1f6dfcc2175647e580be454832d2afd9
Source dataset
uspto-grants-1980_06
Patent number
US04207234

Reaction notes

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