New learning discoveries about 15441-10-8

According to the analysis of related databases, 15441-10-8, the application of this compound in the production field has become more and more popular.

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. 15441-10-8, name is 3-(Aminosulfonyl)propanoic acid, This compound has unique chemical properties. The synthetic route is as follows., Computed Properties of C3H7NO4S

3-sulfamoylpropionic acid (Compound 1) (15.0 g, 97.94 mmol) and 2,4-dihydroxybenzoic acid (Compound 2)(10.2 g, 66.18 mmol) were dissolved in acetic anhydride (22.6 mL). Triethylamine (13.2 mL) was carefully addedto the mixture, andthe mixture was heated for 4 hr.After the reaction, it was cooled and diluted with water.The precipitated product was filtered and washed with aqueous methanol togive (7-hydroxy-2-oxo-2H-chromen-3-yl)methanesulfonamide (Compound 3), 21.2 g, yield 85%.

According to the analysis of related databases, 15441-10-8, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Zeng Qingqiang; (12 pag.)CN108586445; (2018); A;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Extended knowledge of 15441-10-8

The synthetic route of 3-(Aminosulfonyl)propanoic acid has been constantly updated, and we look forward to future research findings.

These common heterocyclic compound, 15441-10-8, name is 3-(Aminosulfonyl)propanoic acid, 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. name: 3-(Aminosulfonyl)propanoic acid

General procedure: To a solution of 3-(4-((2-aminopropyl)thio)-1 ,2,5-oxadiazol-3-yl)-4-(3-(difluoromethyl)-4- fluorophenyl)-1 ,2,4-oxadiazol-5(4H)-one hydroiodide (Int 102) (416 mg, 0.81 mmol), HATU (462 mg, 1 .22 mmol) and Et3N (245 mg, 2.43 mmol) in DMF (8 mL) 2- sulfamoylacetic acid (135 mg, 0.97 mmol) was added and the mixture was stirred at rt overnight. EtOAc (20 mL) was added and the mixture was extracted with water (2 x 20 mL). The combined organic layers were dried over anhydrous Na2S0 , filtered and concentrated to dryness. The residue was purified by column chromatography to give the title compound as a white solid.

The synthetic route of 3-(Aminosulfonyl)propanoic acid has been constantly updated, and we look forward to future research findings.

Reference:
Patent; PHENEX DISCOVERY VERWALTUNGS-GMBH; STEENECK, Christoph; KINZEL, Olaf; ANDERHUB, Simon; HORNBERGER, Martin; KLEYMANN, Gerald; HOFFMANN, Thomas; (191 pag.)WO2018/83241; (2018); A1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics