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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269809Generated: October 30, 2026

1,4-Dioxane hydrochloride → 5-[(Piperidin-3-yl)oxy]-1H-indazole

https://huagongshe.com/reaction/1269809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 22933697HCID 22933697—
SolventMethanolHCID 887—
Product5-[(Piperidin-3-yl)oxy]-1H-indazoleHCID 22933470101.2%

Reaction Steps

To a solution of the tert-butyl 3-(1H-indazol-5-yloxy)piperidine-1-carboxylate (150 mg, 0.473 mmol) obtained in Example 376 in methanol (2 ml) was added a 4N-hydrochloric acid-dioxane solution (1 ml) at room temperature. After 3 hours, the mixture thus obtained was concentrated under reduced pressure, and the resulting residue was dissolved in methanol. The resulting solution was adjusted to pH 8 to 9 with a 2M-aqueous sodium hydroxide solution and concentrated under reduced pressure. The residue was purified by a silica gel column chromatography (eluent: chloroform/methanol/chloroform/methanol/(1%-aqueous ammonia)) to obtain 5-(piperidin-3-yloxy)-1H-indazole (104 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-d0b1fc5b89074ca7abb149cf92859a5f
Source noteuspto-grants-2007_04