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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174940Generated: October 31, 2026

HCID 66664617, compound → HCID 68285181, compound

https://huagongshe.com/reaction/2174940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66664617HCID 66664617—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 68285181HCID 68285181—

Reaction Steps

6-bromo-N-(6-methoxypyridin-3-yl)-3-nitroquinolin-4-amine (compound of step 2, 13.3 mmol) was hydrogenated using Raney-Ni (1 g) in THF-MeOH [(1:1), 50 mL] under 40 psi of hydrogen for 4 h at RT. After completion of the reaction, the reaction mixture was filtered through celite and washed with methanol. The filtrate was concentrated and purified (silica gel column, MeOH/CHCl3 as eluent) to obtain the title compound. 1H NMR (300 MHz, DMSO-d6): δ 8.59 (s, 1H), 7.93 (d, J=2.1 Hz, 1H), 7.78 (d, J=8.7 Hz, 3H), 7.47 (dd, J=2.1, 9.0 Hz, 2H), 6.93 (dd, J=3.0, 8.7 Hz, 1H), 6.65 (d, J=9.0 Hz, 1H), 5.42 (s, 2H), 3.85 (s, 3H); MS (m/z): 345.0 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062046B2
Source datasetuspto-grants-2015_06
ORD IDord-673e3b4168c24bf388dca37bc98a3868
Source noteuspto-grants-2015_06