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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993510Generated: October 30, 2026

4-Chloro-6-(4-nitrophenoxy)pyrimidine → 4-((6-Chloropyrimidin-4-yl)oxy)aniline

https://huagongshe.com/reaction/1993510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-(4-nitrophenoxy)pyrimidineHCID 14363850—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product4-((6-Chloropyrimidin-4-yl)oxy)anilineHCID 22613711—

Reaction Steps

4-Chloro-6-(4-nitro-phenoxy)-pyrimidine (Stage 56.2; 3.6 g, 14.3 mmol) dissolved in MeOH (250 mL) is hydrogenated in the presence of Raney-Ni (3 g) at 40° C. for 3 d. The reaction solution is filtred, concentrated under reduced pressure and crystalized from AcOEt/hexane to give the compound of Stage 56.1: M+H=222/224; 1H-NMR (400 MHz, DMSO-d6): 8.62 (s, 1H, piperidinyl), 7.13 (s, 1H, piperidinyl), 6.83 (d, 9 Hz, 2H, phenyl), 6.56 (d, 9 Hz, 2H, phenyl), 5.12 (s, 2H, NH2); m.p.=135.5-138.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652022B2
Source datasetuspto-grants-2010_01
ORD IDord-7c2407bda8b94de88d8d9a1e15c82a9d
Source noteuspto-grants-2010_01