Simple exploration of 1228779-96-1

1228779-96-1, The synthetic route of 1228779-96-1 has been constantly updated, and we look forward to future research findings.

1228779-96-1, 3-Nitro-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)benzenesulfonamide is a Tetrahydropyrans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A mixture of 2-((lH-pyrrolo[2,3-b]pyridin-5-yl)oxy)-4-(4-((6-(4- chlorophenyl)spiro[3.5]non-6-en-7-yl)methyl)piperazin-l-yl)benzoic acid (1.75 g, 3 mmol), 3-nitro-4-(((tetrahy(ko-2H-pyran-4-yl)memyl)amino)benzenesulfonamide (1.43 g, 4.5 mmol), EDCI (1.15 g, 6 mmol) and 4-(N,N-cUmemylamino)pyridine (550 mg, 4.5mmol) and dichloromethane (40 ml) was reacted at room temperature for overnight, followed by adding water. The water layer was extracted with dichloromethane. The combined organic layers were washed with brine, concentrated and purified through silica gel column to afford 2-((lH-pyrrolo[2,3-b]pyridin-5- yl)oxy)-4-(4-((6-(4-chlorophenyl)spiro[3.5]non-6-en-7-yl)methyl)piperazin-l-yl)-N- ((3-nitro-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)phenyl)sulf onyl)benzamide ( 1.7 g, 64.4 %) as yellow solid. 1H NMR (400 MHz, Methanol-^) delta 8.70 (d, / = 2.3 Hz, 1H), 8.01 (d, / = 2.7 Hz, 1H), 7.87 (d, J = 9.2, 2.3 Hz, 1H), 7.66 (d, / = 8.9 Hz, 1H), 7.55 (d, / = 2.7 Hz, 1H), 7.47 (d, / = 3.4 Hz, 1H), 7.38 (d, / = 8.4 Hz, 2H), 7.10 (d, / = 8.4 Hz, 2H), 6.97 (d, / = 9.2 Hz, 1H), 6.77 (dd, / = 8.9, 2.4 Hz, 1H), 6.44 (d, / = 3.4 Hz, 1H), 6.34 (d, / = 2.4 Hz, 1H), 4.02 – 3.94 (m, 3H), 3.66 (s, 3H), 3.49 – 3.38 (m, 2H), 3.41 – 3.25 (m, 7H), 2.42 (s, 3H), 2.26 (s, 3H), 2.00 – 1.67 (m, 4H), 1.45 – 1.38 (m, 2H).

1228779-96-1, The synthetic route of 1228779-96-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; THE REGENTS OF THE UNIVERSITY OF MICHIGAN; WANG, Chia, Wei; CHEN, Jianyong; (131 pag.)WO2018/27097; (2018); A1;,
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