3-Bromobenzoic acid → 3-bromo-N-(1-propyl-1H-tetrazol-5-yl)benzamide
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=O.[CH2:11]([N:14]1[C:18]([NH2:19])=[N:17][N:16]=[N:15]1)[CH2:12][CH3:13]>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH:19][C:18]1[N:14]([CH2:11][CH2:12][CH3:13])[N:15]=[N:16][N:17]=1)=[O:7]Participants
3
Procedure
Employing 0.25 g (1.2 mmol) of 3-bromo-benzoic acid and 0.16 g (1.2 mmol) of 1-propyl-1H-tetrazol-5-amine in the procedure described above and elution with CH2Cl2/MeOH/Et3N (9.8:0.1:0.1) gave the product in 34% yield.
Workup
- washelution with CH2Cl2/MeOH/Et3N (9.8:0.1:0.1)
- customgave the product in 34% yield
Sources & evidence
- ORD record
- ord-a38095c189cd4a72a2715d4ef3d17980
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975288B2
Reaction notes
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