3-Cyanobenzoic acid → HCID 178522130, compound

HRID 2074031Notes

Reaction equation

HRID 2074031 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH2:16].[C:20]([C:22]1[CH:23]=[C:24]([CH:28]=[CH:29][CH:30]=1)[C:25]([OH:27])=O)#[N:21].[NH:31]1C=N[N:33]=[N:32]1>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH:16][C:25]([C:24]1[CH:23]=[C:22]([C:20]2[NH:21][N:33]=[N:32][N:31]=2)[CH:30]=[CH:29][CH:28]=1)=[O:27]

Participants

4

Reactant 3

HCID 158753-Cyanobenzoic acidHCID 13688376HCID 13688376, compoundHCID 178418441HCID 178418441, compound

Product 1

HCID 178522130HCID 178522130, compound

Procedure

When the procedure of Example 64 is followed and 3-(2-quinolinylmethyloxy)aniline is used in place of 3-amino-benzonitrile and 3-cyanobenzoic acid is used in place of 3-(2-quinolinylmethyloxy) benzoic acid, then the product prepared is 5-(3-(2-quinolinylmethyloxy)anilinocarbonyl)phenyl)tetrazole.

Workup

  1. customthe product prepared

Sources & evidence

ORD record
ord-51b8b84f0e304bbc821988e82db8daa6
Source dataset
uspto-grants-1990_04
Patent number
US04920132

Reaction notes

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