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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846767Generated: November 1, 2026

tert-butyl (3-((3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamate → tert-butyl (3-((3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamate

https://huagongshe.com/reaction/1846767

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3-((3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamateHCID 58548508—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl (3-((3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamateHCID 5854863795%

Reaction Conditions

Temperature30 °C

Reaction Steps

A mixture of tert-butyl (3-((3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamate (346 mg, 1 mmol) and wet Pd—C (50%, 200 mg) in MeOH (100 mL) was stirred under H2 (40 psi) at 30° C. overnight then the reaction mixture was filtered through CELITE® and washed with MeOH. The filtrate was concentrated to give tert-butyl (3-((3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)oxy)cyclobutyl)carbamate (331 mg, 0.95 mmol, yield 95%). ESI-MS (M+1): 349 calc. for C19H28N2O4 348.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952037B2
Source datasetuspto-grants-2015_02
ORD IDord-519643181864489aaac7a0f4b8544aba
Source noteuspto-grants-2015_02