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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958194Generated: October 26, 2026

1,4-Dioxane → 5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-ylamine

https://huagongshe.com/reaction/1958194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant[5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-yl]-carbamic acid tert-butyl esterHCID 68071757—
SolventHydrochloric AcidHCID 313—
Product5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-ylamineHCID 6728114446.9%

Reaction Steps

[5-(4-Chloro-phenyl)-6-cyclobutoxy-pyridin-3-yl]-carbamic acid tert-butyl ester (1.042 g, 2.78 mmol) was dissolved in 4M HCl in dioxane (10.4 ml, 41.7 mmol). The reaction mixture was a light yellow solution and was stirred at room temperature for 1 h. The mixture was partitioned between ethyl acetate and 1M Na2CO3 solution. The organic phases were combined, dried with MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 100 g, 5% to 75% ethyl acetate in heptane) to give 0.358 g (46.9%) of the title compound as light red oil; LC-MS (UV peak area/ESI) 94.3%, 275.0950 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410107B2
Source datasetuspto-grants-2013_04
ORD IDord-c846f2c4743045c18923962498ce0f75
Source noteuspto-grants-2013_04