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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602456Generated: October 31, 2026

Hydrochloric Acid → N-{cis-6-[(4-Hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-3-yl}-1-isopropyl-1H-indazole-3-carboxamide

https://huagongshe.com/reaction/602456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-Butyl cis-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]-5-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}piperidine-1-carboxylateHCID 67270163—
SolventMethanolHCID 887—
ProductN-{cis-6-[(4-Hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-3-yl}-1-isopropyl-1H-indazole-3-carboxamideHCID 67270191106.6%

Reaction Steps

The mixture of tert-butyl cis-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]-5-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}piperidine-1-carboxylate (292 mg, 0.583 mmol, step 6 of Example 2) and 10% hydrochloric acid in methanol (3 mL) was stirred at room temperature for 20 h. The mixture was concentrated under reduced pressure and the resulting residue was dissolved in dichloromethane/methanol (10/1, 10 mL). The solution was filtered through amine-silica gel washing with dichloromethane/methanol (10/1, 200 mL). The filtrate was concentrated under reduced pressure and the resulting residue was chromatographed on a column of silica gel eluting with dichloromethane/methanol/25% ammonium hydroxide (10:1:0.2) to give 249 mg (99%) of the title compound as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906532B2
Source datasetuspto-grants-2011_03
ORD IDord-66b27315a6614e72b96ac1613b645e30
Source noteuspto-grants-2011_03