Water → 3-(3,5-Dibromo-4-hydroxyphenyl)-N-(3-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole-5-carboxamide
Reaction equation
C[Al](C)C.[F:5][C:6]([F:16])([F:15])[O:7][C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][CH:14]=1)[NH2:11].[Br:17][C:18]1[CH:19]=[C:20]([C:26]2[N:30]=[C:29]([C:31](OCC)=[O:32])[O:28][N:27]=2)[CH:21]=[C:22]([Br:25])[C:23]=1[OH:24].O>CCCCCC.C1(C)C=CC=CC=1>[Br:25][C:22]1[CH:21]=[C:20]([C:26]2[N:30]=[C:29]([C:31]([NH:11][C:10]3[CH:12]=[CH:13][CH:14]=[C:8]([O:7][C:6]([F:15])([F:16])[F:5])[CH:9]=3)=[O:32])[O:28][N:27]=2)[CH:19]=[C:18]([Br:17])[C:23]=1[OH:24]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Trimethylaluminum (0.075 mL of a 2 M solution in hexane, 0.15 mmol) was added to a stirred solution of 3-(trifluoromethoxy)aniline (26 mg, 0.15 mmol) in dry toluene (1 mL) under nitrogen. After stirring at room temperature for 1 hour, ethyl 3-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-5-carboxylate (58 mg, 0.15 mmol) was added in one portion and the mixture was stirred at room temperature for three days. Water (1 mL) was added and the mixture was extracted with ethyl acetate (3 mL). The organic phase was evaporated in vacuo to give a colourless oil which was purified by preparative HPLC to give the title compound (23 mg, 31%) as a colourless powder. 1H NMR δ (ppm) (DMSO-d6): 7.22 (1H, d), 7.69 (1H, t), 7.91 (1H, d), 7.98 (1H, s), 10.96 (1H, s, br), 11.97 (1H, s). LCMS (10 cm_apci_formic) tR 4.37 min; m/z 520/522/524 [M−H]−.
Workup
- stirringthe mixture was stirred at room temperature for three days
- extractionthe mixture was extracted with ethyl acetate (3 mL)
- customThe organic phase was evaporated in vacuo
- customto give a colourless oil which
- customwas purified by preparative HPLC
Sources & evidence
- ORD record
- ord-e5bac8d986514b5d8f7cbdf440f27af8
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08207205B2
Reaction notes
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