{"id":5459,"date":"2021-07-21T06:26:02","date_gmt":"2021-07-20T22:26:02","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=5459"},"modified":"2021-07-21T06:26:02","modified_gmt":"2021-07-20T22:26:02","slug":"sources-of-common-compounds-c4h3n3","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=5459","title":{"rendered":"Sources of common compounds: C4H3N3"},"content":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/31108-57-3.html\">Synthetic Route of 31108-57-3<\/a>,Some common heterocyclic compound, 31108-57-3, name is 1H-Pyrazole-4-carbonitrile, molecular formula is C4H3N3, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.<\/p>\n<p>To a solution of I-BA10 (20 mg, 0.047 mmol) in acetone (2 mL) were added K2C03 (13 mg, 0.1 mmol) and lH-pyrazole-4-carbonitrile (9 mg, 0.1 mmol) at l5C. The reaction mixture was stirred for lh at l5C. The reaction mixture was filtered and the mother liquor was concentrated. The residue was purified by flash column (0-30% of EtOAc in PE) to give I- BA11 (10.3 mg, 50%) as a solid. (2459) The structure was confirmed by NOE. (2460) 1H NMR (400 MHz, CDCl3) dH 7.86 (s, 1H), 7.81 (s, 1H), 5.10-4.90 (m, 2H), 2.60 (d, J= 8.8 Hz, 1H), 2.00-1.58 (m, 12H), 1.51-1.28 (m, 11H), 1.26 (s, 3H), 1.24-1.12 (m, 2H), 1.10 (s, 3H), 1.08-0.85 (m, 3H); MS ESI calcd. for C27H38N30 [M+H-H20]+ 420, found 420<\/p>\n<p>The synthetic route of 31108-57-3 has been constantly updated, and we look forward to future research findings.<\/p>\n<p>Reference:<br \/><a href=\"http:\/\/v3.espacenet.com\/textdoc?DB=EPODOC&#038;IDX=WO2019126761&#038;F=0\">Patent; SAGE THERAPEUTICS, INC.; ROBICHAUD, Albert, Jean; SALITURO, Francesco, G.; BLANCO-PILLADO, Maria, Jesus; LA, Daniel; HARRISON, Boyd, L.; (646 pag.)WO2019\/126761; (2019); A1;<\/a>,<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The synthetic route of 31108-57-3 has been constantly updated, and we look forward to future research findings.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[326,131],"tags":[145],"class_list":["post-5459","post","type-post","status-publish","format-standard","hentry","category-31108-57-3","category-pyrazoles-derivatives","tag-m-w0-100"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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