Ethanol → HCID 131713475, compound
Reaction equation
C(O)C.[CH3:4][N:5]1[C:9]([S:10][CH2:11][C:12]2[CH2:13][S:14][C@@H:15]3[CH:22]([NH:23][C:24](=[O:39])[C:25]([C:33]4[N:34]=[C:35]([NH2:38])[S:36][CH:37]=4)=[N:26][O:27][CH2:28][CH2:29][N:30]=[N+:31]=[N-:32])[C:21](=[O:40])[N:16]3[C:17]=2[C:18]([OH:20])=[O:19])=[N:8][N:7]=[N:6]1.C(=O)(O)[O-].[Na+:45]>O>[CH3:4][N:5]1[C:9]([S:10][CH2:11][C:12]2[CH2:13][S:14][C@@H:15]3[CH:22]([NH:23][C:24](=[O:39])[C:25]([C:33]4[N:34]=[C:35]([NH2:38])[S:36][CH:37]=4)=[N:26][O:27][CH2:28][CH2:29][N:30]=[N+:31]=[N-:32])[C:21](=[O:40])[N:16]3[C:17]=2[C:18]([O-:20])=[O:19])=[N:8][N:7]=[N:6]1.[Na+:45]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1 ml of ethanol was added to a solution of 0.162 g of the product of Example 36 in 0.3 ml of a molar solution of sodium bicarbonate in water and the mixture was vacuum filtered. The filtrate was evaporated to dryness undere reduced pressure and the residue was taken up in ethanol. After efflorescence, the mixture was vaccum filtered to obtain 0.09 g of the syn isomer of sodium 3-[(1-methyl-1H-tetrazol-5-yl)-thiomethyl]-7-[2-(2-amino-4-thiazolyl)-2-(2-azidoethoxyimino)-acetamido]-ceph-3-eme-4-carboxylate.
Workup
- filtrationfiltered
- customThe filtrate was evaporated to dryness undere reduced pressure
- filtrationAfter efflorescence, the mixture was vaccum filtered
Sources & evidence
- ORD record
- ord-9b7ce19e658b443ab58da3e990f4a22c
- Source dataset
- uspto-grants-1984_03
- Patent number
- US04439433
Reaction notes
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