{"id":4118,"date":"2021-05-18T03:48:33","date_gmt":"2021-05-17T19:48:33","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=4118"},"modified":"2021-05-18T03:48:33","modified_gmt":"2021-05-17T19:48:33","slug":"some-tips-on-56-dihydro-4h-pyrrolo12-bpyrazole-2-carboxylic-acid","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=4118","title":{"rendered":"Some tips on 5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylic acid"},"content":{"rendered":"

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 796729-03-8, name is 5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylic acid, A new synthetic method of this compound is introduced below., Quality Control of 5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylic acid<\/a><\/p>\n

Example 133N-((ls,4s)-4-(5-fluoro-2-(4′-(3-(piperazin-l-yl)propyl)biphenyl-3- yloxy)nicotinamido)cyclohexyl)-5,6-dihydro-4H-pyrrolo[l,2-b]pyrazole-2-carboxamide To a solution of tert-butyl 4-(3-(3′-(3-((ls,4s)-4-aminocyclohexylcarbamoyl)-5-fluoropyridin- 2-yloxy)biphenyl-4-yl)propyl)piperazine-l-carboxylate (150 mg, 0.24 mmol) in acetonitrile (2 mL) was added 5,6-dihydro-4H-pyrrolo[l,2-b]pyrazole-2-carboxylic acid (36.1 mg, 0.24 mmol) and triethylamine (0.331 mL, 2.37 mmol). 1-Propanephosphonic acid cyclic anhydride, 1.57M solution in THF (0.159 mL, 0.25 mmol) was then added and the mixture stirred at RT for 1 h. The mixture was poured into sat NaHCO3 (aq) and the organics extracted into EtOAc (x2). The extractions were combined, dried (MgSO4) and evaporated to give a residue. This was dissolved in DCM (2mL) to which TFA (2mL) was added and the mixture stirred at RT for 20 min. The solvents were removed in vacuo and the residue dissolved in methanol and purified using reverse phase preparative chromatography using eluent = TFA(aq)\/MeOH. The appropriate fractions were combined and evaporated to give a residue which on trituration with ether gave a solid. The solid was dried overnight under vacuum at 400C to give the title compound. Yield: 48 mg1H NMR (400 MHz, CD3OD) 5 8.45 (d, J= 7.2 Hz, IH), 8.11 (d, J= 3.1 Hz, IH), 8.05 (dd, J = 7.9, 3.1 Hz, IH), 7.51 (d, J= 8.2 Hz, 2H), 7.47 (d, J= 5.1 Hz, 2H), 7.40 – 7.39 (m, IH), 7.24 (d, J= 8.2 Hz, 2H), 7.15 – 7.12 (m, IH), 6.39 (s, IH), 4.14 – 4.07 (m, IH), 4.03 (t, J= 7.3 Hz, 2H), 3.99 – 3.92 (m, IH), 3.41 (t, J= 5.1 Hz, 4H), 3.24 – 3.19 (m, 4H), 2.95 – 2.90 (m, 2H), 2.87 (t, J= 7.3 Hz, 2H), 2.71 (t, J= 7.4 Hz, 2H), 2.61 – 2.53 (m, 2H), 2.04 – 1.95 (m, 2H), 1.87 – 1.77 (m, 6H), 1.73 – 1.64 (m, 2H). MS: [M+H]+=666 (calc=666) (MultiMode+)<\/p>\n

The synthetic route of 796729-03-8 has been constantly updated, and we look forward to future research findings.<\/p>\n

Reference:
Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2009\/144494; (2009); A1;<\/a>,
Pyrazole – Wikipedia<\/a>,
Pyrazoles – an overview | ScienceDirect Topics<\/p>\n","protected":false},"excerpt":{"rendered":"

The synthetic route of 796729-03-8 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":[602,131],"tags":[126],"class_list":["post-4118","post","type-post","status-publish","format-standard","hentry","category-796729-03-8","category-pyrazoles-derivatives","tag-m-w100-200"],"yoast_head":"\nSome tips on<\/title>\n<meta name=\"description\" content=\"Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. 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