Author: Jessica.F

Adding a certain compound to certain chemical reactions, such as: 391-12-8, name is 7-(Trifluoromethyl)isatin, belongs to indolines-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 391-12-8, Product Details of 391-12-8

General procedure: Isatin (0.5 g, 3.34 mmol) was added into a stirred solution ofKOH (0.56 g, 10.02 mmol) in ethanol 10 ml at 80 C. The reactionmixture was stirred at 0 C for 24 h. The mixture was added to50 g ice water. The pH was adjusted by the solution of 2 N HCl to4?5. The mixture was cooled overnight and filtered. The residuewas recrystallized by the mixture of petroleum/ethyl acetate(5:1). Compound 4 (0.8 g) was obtained and the yield was 96.87percent.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 7-(Trifluoromethyl)isatin, and friends who are interested can also refer to it.

Reference:
Article; Liao, Chen; Liu, Yan; Liu, Chunxia; Zhou, Jiaqi; Li, Huilan; Wang, Nasi; Li, Jieming; Liu, Taiyu; Ghaleb, Hesham; Huang, Wenlong; Qian, Hai; Bioorganic and Medicinal Chemistry; vol. 26; 4; (2018); p. 845 – 854;,
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In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 317-20-4 as follows. SDS of cas: 317-20-4

General procedure: Isatins (1a-j, 3.0 g), hydrazine hydrate (80%, 13 mL) and water (13 mL) were added to a flask equipped with a thermometer with vigorous stirring. The reaction mixture was kept at 140 C in an oil bath for 6 h before being cooled to r.t., when hydrochloric acid (2.0 mol L-1) was added to bring the pH to pH 2. The reaction mixture was stirred at r.t. for 12 h. Compounds 2a-j were obtained by filtering under vacuum and recrystallisation from absolute ethanol.

According to the analysis of related databases, 317-20-4, the application of this compound in the production field has become more and more popular.

Reference:
Article; Zhang, Chao; Xu, Juan; Zhao, Xinyu; Kang, Congmin; Journal of Chemical Research; vol. 41; 9; (2017); p. 537 – 540;,
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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. 5428-09-1, name is 2-Allylisoindoline-1,3-dione, A new synthetic method of this compound is introduced below., Formula: C11H9NO2

Under nitrogen atmosphere, in 250 ml adding three-necked bottle 9.35g (0.05mol) A1 and 150 ml benzene, after stirring to dissolve by adding 0.2 ml the mass fraction is 0.520percent of the Karstedt catalyst is, 50 ¡ãC activated 30 min, then add 8.2g (0.05mol) triethoxy silane, the temperature is increased to 70 ¡ãC, reaction 10h evaporating the solvent to obtain gray oily liquid, using dichloromethane: methanol = 1:3(V/V) column to obtain the product (A2) 16.2g, yield of 92.5percent.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; Nanchang University; Qi, Haixia; Fu, Zhiqiang; Zhang, Yubao; Liu, Feng; (7 pag.)CN105669738; (2016); A;,
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Electric Literature of 20870-79-5, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 20870-79-5 name is 5-Nitroindolin-2-one, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

To a solution of 5-nitro-oxindole (25 g) in 120 mL of dimethylacetamide in a Parr bottle was added 10% Pd/C (0.5 g). The mixture was hydrogenated (40 psi H2) for 16 hours. The catalyst was removed by filtration and the filtrate was diluted with ether (2 L) to provide 5-amino-oxindole (10.5 g; 50%).

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 5-Nitroindolin-2-one, and friends who are interested can also refer to it.

Reference:
Patent; Pfizer Inc; US2005/256144; (2005); A1;,
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20780-72-7, name is 4-Bromoisatin, belongs to indolines-derivatives compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. Quality Control of 4-Bromoisatin

General procedure: At first, 0.5mmol of aryl aldehyde or isatin was added to a mixture of ketone (cyclohexanone or acetone, 5equiv), 15 or 20molpercent catalyst, 30 or 40molpercent acid, and 2.0mL of solvent at reaction temperature. The reaction mixture was stirred for the indicated time and then purified through flash column chromatography on a silica gel (petroleum ether/ethyl acetate) to afford the pure products.

The synthetic route of 20780-72-7 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Xu, Biao; Li, Lei; Gou, Shaohua; Tetrahedron Asymmetry; vol. 24; 24; (2013); p. 1556 – 1561;,
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Some common heterocyclic compound, 101207-45-8, name is 2-(4-Methylbenzyl)isoindoline-1,3-dione, molecular formula is C16H13NO2, 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. Product Details of 101207-45-8

REFERENTIAL EXAMPLE 11 To 50.3 g of 4-phthalimidomethyltoluene, were added 39 g of N-bromosuccinimide (NBS), 1.5 g of benzoyl peroxide (BPO), and 500 ml of carbon tetrachloride. The mixture was heated under reflux for one hour. The reaction mixture was cooled in ice, filtered from insolubles, and concentrated under reduced pressure. The residue was recrystallized from methanol to yield 40 g of colorless needle crystals of 4-phthalimidomethylbenzyl bromide; m.p. 129-131 C.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 101207-45-8, its application will become more common.

Reference:
Patent; Torii & Co. Ltd.; US4598077; (1986); A;,
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These common heterocyclic compound, 3891-07-4, name is 2-(2-Hydroxyethyl)isoindoline-1,3-dione, its 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. category: indolines-derivatives

To a mechanically stirred suspension of NaH (15g, 0. 375 mol, 60% dispersion in mineral oil) in THF (250 mL) and DMF (25 mL) was added N- (2-hydroxyethyl)-phtalimide (43g, 0. 225 mol). The mixture was stirred at room temperature for about 4 h and then cooled to about 0C in an ice bath. Ethyl-4- chloroacetate (21. 4 mL, 0. 15 mol) in THF (4 mL) was then added via an addition funnel over a period of about 0. 5 h and the resulting mixture allowed to stir overnight. The mixture was then poured into a 2 L sepratory funnel containing 500 mL ice water and 700 mL EtOAc and separated. The organic layer was washed 2x with 500 mL of water and dried over MGS04. The solution was then filtered through a 4-inch plug of silica and then CONCENTRATED IN VACUO. The resulting yellow oil was then dissolved in 250 mL CH3CN and washed 2x with 30 mL hexane. The CH3CN layer was the concentrated in vacuo to yield 19. 4g (40. 5%) OF 4- [2- (1, 3-DIOXO-1, 3-DIHYDRO-ISOINDOL-2-YL)-ETHOXY]-3-OXO-BUTYRIC acid ethyl ester as a yellow oil. This crude compound was used for the next step

The synthetic route of 2-(2-Hydroxyethyl)isoindoline-1,3-dione has been constantly updated, and we look forward to future research findings.

Reference:
Patent; SYNTA PHAMACEUTICALS CORP.; WO2005/25507; (2005); A2;,
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Related Products of 39755-95-8, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 39755-95-8, name is 5-Methoxyisatin, This compound has unique chemical properties. The synthetic route is as follows.

Intermediate 20: 5-Methoxyindolin-2-one[0507] A solution of 5-methoxyisatin (1.0 g, 5.6 mmol) in hydrazine hydrate (85%, 6.0 mL) was refluxed for 3 h. After the mixture was concentrated, the residue was treated with 50%> aqueous NaOH solution (40.0 mL) and the resulting mixture was stirred at room temperature for 48 h. The mixture was poured into water and extracted with diethyl ether. The combined extracts were washed with brine, dried over anhydrous Na2S04 and concentrated. The residue was purified by flash column chromatography (PE/EA = 10: 1 to 2:1) to afford 184 mg of the title compound as a white solid (20% yield).

The chemical industry reduces the impact on the environment during synthesis 5-Methoxyisatin. I believe this compound will play a more active role in future production and life.

Reference:
Patent; ZENOBIA THERAPEUTICS, INC.; BOUNAUD, Pierre-Yves; NIENABER, Vicki; STEENSMA, Ruo, W.; LOWE, John, A., III; WO2012/178015; (2012); A2;,
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Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 86626-38-2, name is 4-Bromoindoline, This compound has unique chemical properties. The synthetic route is as follows., Quality Control of 4-Bromoindoline

A mixture of above obtained 4-bromoindoline (759 mg, 3.81 mmol), and (Boc)20 (976 mg, 4.48 mmol) in MeCN (8 mL) was stirred at room temperature overnight. After evaporated, the residue was dissolved in ethyl acetate (40 mL), washed with water (3 x 20 mL) and brine (1 x 20 mL). The organic layer was concentrated and purified by column chromatography on silica gel (petroleum ether) to give 0601-177(840 mg, 74%>) as a white solid. 1H-NMR (400 MHz. DMSO-Patent; CURIS, INC.; BAO, Rudi; LAI, Chengjung; QIAN, Changgeng; WO2011/130628; (2011); A1;,
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In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 118289-55-7 as follows. COA of Formula: C10H9Cl2NO

Example 1 6-chloro-5-(2-(4-(2,3-dihydrobenzo[b]thiophen-4-yl)piperazin-1-yl)ethyl)indolin-2-one 6-chloro-5-(2-chloroethyl)indolin-2-one (120 mg, 0.52 mmol), the product of Reference Example 12 (115 mg, 0.52 mmol), potassium carbonate (215 mg, 1.56 mmol), potassium iodide (86 mg, 0.52 mmol) and acetonitrile (5 ml) were added to the flask and the mixture was stirred at 85 C. overnight. The reaction mixture was concentrated and subjected to column chromatography to obtain a white solid (120 mg, yield: 56%). 1HNMR (300 MHz, DMSO-d6): delta ppm 10.42 (brs, 1H), 7.21 (s, 1H), 7.07 (t, 1H), 6.90 (d, 1H), 6.80 (s, 1H), 6.69 (d, 1H), 3.45 (s, 2H), 3.30 (t, 2H), 3.14 (t, 2H), 2.74-2.95 (m, 6H), 2.59 (brs, 4H), 2.50 (t, 2H). ESI-MS (m/z): 414.2 [M+H]+.

According to the analysis of related databases, 118289-55-7, the application of this compound in the production field has become more and more popular.

Reference:
Patent; SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES; SUZHOU VIGONVITA LIFE SCIENCES CO., LTD.; TOPHARMAN SHANDONG CO., LTD.; JIANG, Hualiang; WANG, Zhen; LI, Jianfeng; ZHANG, Rongxia; HE, Yang; LIU, Yongjian; BI, Minghao; LIU, Zheng; TIAN, Guanghui; CHEN, Weiming; YANG, Feipu; WU, Chunhui; WANG, Yu; JIANG, Xiangrui; YIN, Jingjing; WANG, Guan; SHEN, Jingshan; (70 pag.)US2017/158680; (2017); A1;,
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