Category: 196799-45-8

Analyzing the synthesis route of 196799-45-8

The synthetic route of 196799-45-8 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.196799-45-8,2,3-Dihydrobenzofuran-7-carbaldehyde,as a common compound, the synthetic route is as follows.

(4′-(Pyridin-2-yl)tetrahydrospiro[bicyclo[3.1.0]hexane-3,2′-pyran]-4′-yl)ethylamine (68E) (0.22 g, 0.808 mmol) dissolved in dichloromethane (10 mL)In the middle, sodium sulfate (0.57g, 4.04mmol)And 2,3-dihydrobenzofuran-7-carbaldehyde (0.144 g, 0.97 mmol) was added to the reaction.The reaction was carried out overnight at room temperature. Sodium borohydride(0.046 g, 1.10 mmol) was added to the reaction, and the reaction was stirred for 10 minutes.Further methanol (10 mL) was added and the reaction was stirred for 1 hour.The reaction was quenched with water and aqueous was extracted with dichloromethane (20mL¡Á3).The combined organic phases were washed with a saturated sodium chloride solution (30 mL).Dry with anhydrous sodium sulfate, filter, and concentrate the filtrate.Column chromatography on crude product (dichloromethane/methanol (v/v) = 50:1 to 20:1)Obtaining a yellow oily liquidN-((2,3-dihydrobenzofuran-7-yl)methyl)-2-(4′-(pyridin-2-yl)tetrahydrospiro[bicyclo[3.1.0]hexane-3, 2′-pyran]-4′-yl)ethylamine (76B) (0.22 g, yield: 67.5%)., 196799-45-8

The synthetic route of 196799-45-8 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Sichuan Hai Sike Pharmaceutical Co., Ltd.; Fan Jiang; Zhu Fengfei; Chen Qingping; Wang Chengtao; (251 pag.)CN109206417; (2019); A;,
Benzofuran – Wikipedia
Benzofuran | C8H6O – PubChem

Simple exploration of 196799-45-8

196799-45-8, 196799-45-8 2,3-Dihydrobenzofuran-7-carbaldehyde 2795018, abenzofuran compound, is more and more widely used in various fields.

196799-45-8, 2,3-Dihydrobenzofuran-7-carbaldehyde is a benzofuran compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

2,3-Dihydro-benzofuran-7-carbaldehyde (1.50 g, 10.20 mmol) was dissolved in ether, then cooled to 0 C., NaBH4 (400 mg, 10.57 mmol) in MeOH (5.00 mL) was added. The resulting reaction mixture was stirred for 30 min, then saturated ammonium chloride was added. The mixture was extracted with ether, and the combined organic phases were washed with brine, then dried over magnesium sulfate and concentrated to afford the desired alcohol

196799-45-8, 196799-45-8 2,3-Dihydrobenzofuran-7-carbaldehyde 2795018, abenzofuran compound, is more and more widely used in various fields.

Reference£º
Patent; Allergan, Inc.; US2008/255230; (2008); A1;,
Benzofuran – Wikipedia
Benzofuran | C8H6O – PubChem

New learning discoveries about 196799-45-8

As the paragraph descriping shows that 196799-45-8 is playing an increasingly important role.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.196799-45-8,2,3-Dihydrobenzofuran-7-carbaldehyde,as a common compound, the synthetic route is as follows.

General procedure: Et3N (1.0 equiv) was added to a suspension of 2-(4-bromo-2,5-dimethoxyphenyl)ethanamine hydrochloride (2C-B*HCl, 1.0 mmol) and the required aldehyde (1.1 equiv) in EtOH (10 mL) and the reaction was stirred until formation of the imine was complete according to TLC or GC (between 30 min and 3 h depending on the aldehyde). NaBH4 (2.0 mmol) was then added and the reactionwas stirred for another 30 min. The reaction mixture was concentratedunder reduced pressure and the residue was partitioned between CH2Cl2 and water (30 mL, 1:1). The organic layer was isolated and the aqueous layer was extracted with CH2Cl2 (2 x 15 mL). The combined organic extracts were dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography (CH2Cl2/MeOH/NH3 98:2:0.04). The purified free base was dissolved in EtOH (2 mL) and HCl (1 M in EtOH, 2 mL) was added and the resulting solution was diluted with Et2O until a precipitate was formed. The crystals were collected by filtration and dried under reduced pressure to provide the desired products.

As the paragraph descriping shows that 196799-45-8 is playing an increasingly important role.

Reference£º
Article; Hansen, Martin; Jacobsen, Stine Engesgaard; Plunkett, Shane; Liebscher, Gudrun Eckhard; McCorvy, John D.; Braeuner-Osborne, Hans; Kristensen, Jesper Langgaard; Bioorganic and Medicinal Chemistry; vol. 23; 14; (2015); p. 3933 – 3937;,
Benzofuran – Wikipedia
Benzofuran | C8H6O – PubChem