HCID 20297252, compound → HCID 178454486, compound

HRID 1389608Notes

Reaction equation

HRID 1389608 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH:10]([CH2:14][CH3:15])[C:11]([OH:13])=O)=[O:9])=[CH:4][CH:3]=1.[NH2:16][CH:17]1[C:35](=[O:36])[N:19]2[C:20]([C:32]([OH:34])=[O:33])=[C:21]([CH:24]([S:26][C:27]3[NH:31][N:30]=[N:29][N:28]=3)[CH3:25])[CH2:22][S:23][C@H:18]12>>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([CH:10]([CH2:14][CH3:15])[C:11]([NH:16][CH:17]2[C:35](=[O:36])[N:19]3[C:20]([C:32]([OH:34])=[O:33])=[C:21]([CH:24]([S:26][C:27]4[NH:28][N:29]=[N:30][N:31]=4)[CH3:25])[CH2:22][S:23][C@H:18]23)=[O:13])=[O:9])=[CH:6][CH:7]=1

Participants

3

Procedure

456 mg. of 2-(p-hydroxyphenylsulfinyl)butyric acid and 7-amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid were reacted in the same manner as described in Example 28 and 237 mg. of 7-[2-(p-hydroxyphenylsulfinyl)butyramido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid were obtained.

Sources & evidence

ORD record
ord-07f301548dbe46c1b9c6f7877fb61adc
Source dataset
uspto-grants-1981_01
Patent number
US04245107

Reaction notes

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