Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611160Generated: November 2, 2026

1,4-Dioxane hydrochloride → HCID 135550604, compound

https://huagongshe.com/reaction/1611160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 135550623HCID 135550623—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 135550604HCID 13555060488%

Reaction Steps

To a solution of tert-butyl 3-{2-amino-6-[2-(benzyloxy)-6-hydroxyphenyl]-3-cyano-4-pyridinyl}-1-piperidinecarboxylate (239 mg, 0.48 mmol) in dioxane (25 mL) was added 4N HCl/dioxane (25 mL). The reaction mixture was stirred at room temperature overnight. The resulting precipitate was collected by filtration, washed with ethyl acetate and hexane, dried under reduced pressure to give 2-amino-6-[2-(benzyloxy)-6-hydroxyphenyl]-4-(3-piperidinyl)nicotinonitrile hydrochloride (184 mg, yield; 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-6925cce2994c45f69151152fd52f889d
Source noteuspto-grants-2006_01