HCID 12906743, compound → HCID 23329783, compound

HRID 225320Notes

Reaction equation

HRID 225320 reaction equation
[N:1]([C:4]1[CH:5]=[C:6]([CH2:11][C:12]([OH:14])=O)[CH:7]=[CH:8][C:9]=1[OH:10])=[N+:2]=[N-:3].[NH2:15][C:16]1([O:36][CH3:37])[C:23](=[O:24])[N:22]2[CH:17]1[S:18][CH2:19][C:20]([CH2:28][S:29][C:30]1[S:31][C:32]([CH3:35])=[N:33][N:34]=1)=[C:21]2[C:25]([OH:27])=[O:26]>>[N:1]([C:4]1[CH:5]=[C:6]([CH2:11][C:12]([NH:15][C:16]2([O:36][CH3:37])[C:23](=[O:24])[N:22]3[CH:17]2[S:18][CH2:19][C:20]([CH2:28][S:29][C:30]2[S:31][C:32]([CH3:35])=[N:33][N:34]=2)=[C:21]3[C:25]([OH:27])=[O:26])=[O:14])[CH:7]=[CH:8][C:9]=1[OH:10])=[N+:2]=[N-:3]

Participants

3

Procedure

The title compound is prepared when 3-azido-4-hydroxybenzeneacetic acid is reacted with 7-amino-7-methoxy-3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid according to Procedure V.

Sources & evidence

ORD record
ord-3674d8683d9d433d9eae4086c630f602
Source dataset
uspto-grants-1980_11
Patent number
US04236002

Reaction notes

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