Some tips on 696-42-4

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 696-42-4, 5-Fluoronicotinonitrile.

Reference of 696-42-4, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 696-42-4, name is 5-Fluoronicotinonitrile. This compound has unique chemical properties. The synthetic route is as follows.

[0307] Cesium carbonate (0.734 g, 2.25 mmol) and 5-chloro-3-methylpyridine-2-carbonitrile (0.206 g, 1.35 mmol) wereadded at room temperature to a suspension of the optically active form of cis-1-(diphenylmethyl)-5-hydroxy-3-(piperidin-4-yl)-4-(trifluoromethyl)-1,4,5,7-tetrahydro-6H-pyrazolo[3,4-b]pyridin-6-one (0.212 g, 0.451 mmol) produced in ReferenceExample 27 in DMSO (2 mL), and the mixture was stirred at 150C for 2 hours. The reaction suspension wascooled to room temperature, then diluted with ethyl acetate, and washed with brine. The obtained organic layer wasdried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residuewas purified by silica gel column chromatography [elute: hexane/ethyl acetate = 92/8 – 50/50 (gradient)] to obtain thetitle compound (0.226 g, yield: 86%, optically active form:_[0327] The title compound (42.7 g, yield: 70%, optically active form) was obtained through reaction at 80C for 1 hourand then at 100C for 5 hours by the method described in Reference Example 30 using 5-fluoropyridine-3-carbonitrile(26.0 mg, 0.213 mmol) instead of 5-chloro-3-methylpyridine-2-carbonitrile.[0328] 1H-NMR (400MHz, CDCl3) delta: 8.46 (1H, d, J=3Hz), 8.25 (1H, d, J=2Hz), 7.43-7.04 (10H, m), 6.91 (1H, s), 6.71(1H, s), 4.56-4.51 (1H, m), 3.96-3.86 (1H, m), 3.83-3.73 (2H, m), 3.72-3.67 (1H, m), 3.02-2.93 (2H, m), 2.87-2.76 (1H,m), 2.08-1.85 (4H, m).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 696-42-4, 5-Fluoronicotinonitrile.

Reference:
Patent; Daiichi Sankyo Company, Limited; KOBAYASHI, Hideki; ARAI, Masami; KANEKO, Toshio; TERASAKA, Naoki; (95 pag.)EP3081566; (2016); A1;,
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