The origin of a common compound about Reference of 702-82-9

According to the analysis of related databases, 702-82-9, the application of this compound in the production field has become more and more popular.

Reference of 702-82-9, Adding some certain compound to certain chemical reactions, such as: 702-82-9, name is 3-Aminoadamantan-1-ol,molecular formula is C10H17NO, 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 702-82-9.

EXAMPLESExample 1-1 (General procedure (A))4-(2,4-Dichloro-phenoxy)-N-((1 R,3S,5R,7S)-3-hvdroxy-adamantan-1-yl)-butyramideTo a stirred solution of 4-(2,4-dichloro-phenoxy)-butyric acid (0.8 g, 3.21 mmol) in dry THF (25 mL) was added HOBt (0.48 mg, 3.533 mmol) and EDAC (0.68 g, 3.533 mmol). After stirring for 10 min. at room temperature, DIPEA (0.62 mL) and 3-amino-adamantan-1- ol (0.59 g, 3.533 mmol) were added and the resulting mixture was stirred for 16 hrs. at room temperature. The volatiles were removed in vacuo and to the residue was added water (25 mL) followed by extraction with EtOAc (3×35 mL). The combined organic phases were washed with brine, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The oily residue was crystallised from diethyl ether (5 mL) affording after drying at 50 0C in vacuo 800 mg (62 %) of the title compound as a solid. 1H NMR (400 MHz, DMSO-c/6) delta 1.35 – 1.58 (m, 6H), 1.70 – 1.85 (m, 6H), 1.91 (q, 2H) 2.09 (br.s., 2H), 2.21 (t, 2H), 4.04 (t, 2H), 4.48 (br.s., 1 H), 7.15 (d, 1 H), 7.36 (dd, 1 H), 7.40 (br.s., 1 H), 7.57 (d, 1 H).

According to the analysis of related databases, 702-82-9, the application of this compound in the production field has become more and more popular.

Reference:
Patent; TRANSTECH PHARMA, INC.; NOVO NORDISK A/S; WO2008/134221; (2008); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts