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CAS No. : | 454-92-2 | MDL No. : | MFCD00002519 |
Formula : | C8H5F3O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | FQXQBFUUVCDIRK-UHFFFAOYSA-N |
M.W : | 190.12 | Pubchem ID : | 9963 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20℃; for 48.0h; | A solution of <strong>[45865-42-7]2-amino-5-t-butyl-4-methylthiazole</strong> (1.0 g), 3-(trifluoromethyl)benzoic acid (1.2 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide monohydrochloride (1.2 g) and 1-hydroxybenzotriazole monohydrate (1.0 g) in N,N,-dimethyl formamide (10 ml) was stirred at room temperature for 48 hours. To the reaction solution, ethyl acetate was added and the reaction solution was washed sequentially with 2M hydrochloric acid, an aqueous 2M sodium hydroxide solution, and saturated brine, dried over anhydrous sodium sulfate and filtrated. Thereafter, the filtrate was concentrated under vacuum to obtain a yellow amorphous substance of 5-t-butyl-4-methyl-2-(3-trifluoromethylbenzoyl)aminothiazole (1.7 g). 1H-NMR (200 MHz, CHLOROFORM-D) d ppm; 1.42(s, 9H), 2.20(s, 3H), 7.55 (t, J=7.5 Hz, 1H), 7.78 (d, J=7.5 Hz, 1H), 8.05 (d, J=7.5 Hz, 1H), 8.16 (s, 1H), MS(ESI) (Positive)m/z, 343(M+H) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
14% | With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; | N-(4- (4,4,5, 5-tetramethyl-l,3,2-dioxaborolan-2-yl)naphthalen-l-yl)-3-(trifluoromethyl)benzamide (compound 4). 4-Aminonaphthalene-l-boronic acid pinacol ester (75.0 mg, 0.267 mmol), 3- (Trifluoromethyl)benzoic acid (67.5 mg, 0.348 mmol), HOBt (55.1 mg, 0.348 mmol), EDCI (68.0 mg, 0.348 mmol) and DIPEA (141 mu, 0.803 mmol) were dissolved in DMF (790 mu) and stirred overnight at room temperature. The crude mixture was diluted in ethyl acetate and washed with NH4C1 and Na2C03. The organic layer was dried over Na2S04 and concentrated in vacuo. The crude organic product was purified by column chromatography (20% ethyl acetate in hexanes) to afford 16.6 mg of compound 4 (14% yield). TLC (hexanes:EtOAc, 80:20 v/v): Rf = 0.4; 1H NMR (300 MHz, MeOD) delta 8.87-8.84 (m, 1H), 8.41-8.36 (m, 2H), 8.13-8.04 (m, 2H), 8.01-7.96 (m, 1H), 7.85-7.78 (m, 1H), 7.68 (d, J = 6.0 Hz, 1H), 7.58-7.55 (m, 2H), 1.47 (s, 12H); ESI-MS (m/z): [M]+ calcd. for C24H23BF3N03, 441.17; [M+l]+ found, 442.2. |
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