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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060692Generated: October 31, 2026

Ammonium Chloride → 5-(2-Chloropyridin-4-yloxy)pyridin-2-amine

https://huagongshe.com/reaction/2060692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-4-((6-nitropyridin-3-yl)oxy)pyridineHCID 59322779—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-(2-Chloropyridin-4-yloxy)pyridin-2-amineHCID 59322788103%

Reaction Steps

2-Chloro-4-(6-nitropyridin-3-yloxy)pyridine (0.540 g, 2.146 mmol) was dissolved in THF (54 ml) and MeOH (54 ml). Ammonium chloride (1.148 g, 21.46 mmol) was then added, followed by zinc dust (1.403 g, 21.46 mmol). The reaction was stirred at RT for 45 minutes, filtered over Celite® and concentrated under reduced pressure to yield 5-(2-chloropyridin-4-yloxy)pyridin-2-amine as a brown solid (0.49 g, 99%). It was used as is in the next reaction. 1H NMR (400 MHz, DMSO-d6): δ 8.46 (d, 1H), 7.81 (d, 1H), 7.30 (dd, 1H), 6.90 (m, 2H), 6.50 (d, 1H), 6.08 (s, 2H); MS (ESI) m/z: 222.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278331B2
Source datasetuspto-grants-2012_10
ORD IDord-34a9c2d1f8ba49b08a8ad21fd40e84cf
Source noteuspto-grants-2012_10