1H-1,2,3-Triazole → 3,5-difluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid
Reaction equation
N1N(C2C=CC(C(F)(F)F)=CC=2C(O)=O)N=CC=1.N1(C2C=CC(C(F)(F)F)=CC=2C(O)=O)C=CN=N1.[N:37]1[NH:38][N:39]=[CH:40][CH:41]=1.Br[C:43]1[C:51]([F:52])=[CH:50][C:49]([F:53])=[CH:48][C:44]=1[C:45]([OH:47])=[O:46]>O1CCOCC1.O>[F:52][C:51]1[C:43]([N:38]2[N:39]=[CH:40][CH:41]=[N:37]2)=[C:44]([CH:48]=[C:49]([F:53])[CH:50]=1)[C:45]([OH:47])=[O:46]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepared according to the procedure for 2-(2H-1,2,3-triazol-2-yl)-5-(trifluoromethyl)benzoic acid (Intermediate 37a) and 2-(1H-1,2,3-triazol-1-yl)-5-(trifluoromethyl)benzoic acid (Intermediate 37b) from 2H-1,2,3-triazole (CAS number 288-36-8; 1.0 g, 10.86 mmol) and 2-bromo-3,5-difluorobenzoic acid (CAS number 651027-01-9; 1.27 g, 5.43 mmol) in 1,4-dioxane (5 ml) and water (1 ml). The crude solid was purified by using column chromatography (silica, 0-3% methanol/DCM) to afford 3,5-difluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid (Intermediate 40a). The mixed fractions were further purified by column chromatography (silica, 0-3% methanol/DCM) followed by reverse phase preparative HPLC (eluted with acetonitrile/water containing 0.1% formic acid) to afford 3,5-difluoro-2-(1H-1,2,3-triazol-1-yl)benzoic acid (Intermediate 40b).
Workup
- customPrepared
- customThe crude solid was purified
Sources & evidence
- ORD record
- ord-7fd97785e5d246678b8ed4e3e16e9efe
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09156829B2
Reaction notes
Loading…