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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595932Generated: October 30, 2026

Trifluoroacetic acid → 5-(4-methyltetrahydro-2H-pyran-4-yl)pyridin-2-amine

https://huagongshe.com/reaction/595932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-(2,4-dimethoxybenzyl)-5-(4-methyltetrahydro-2H-pyran-4-yl)pyridin-2-amineHCID 118045285—
SolventDichloromethaneHCID 6344—
Product5-(4-methyltetrahydro-2H-pyran-4-yl)pyridin-2-amineHCID 11804560389.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice cold solution of N-(2,4-dimethoxybenzyl)-5-(4-methyltetrahydro-2H-pyran-4-yl)pyridin-2-amine (100 mg, 0.29 mmol) in DCM (6 mL) was added 10 mL 30% TFA in DCM solution. The resulting solution was stirred at 0° C. for 15 min. The solvent was removed via vacuum. The resulting residue was redissolved in ethyl acetate, and the organic solution was washed with 1M NaOH, brine, dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography on silicagel (ISCO) eluting with 0-100% ethyl acetate in heptane to give 5-(4-methyltetrahydro-2H-pyran-4-yl)pyridin-2-amine (50 mg, 0.26 mmol, 89% yield) as white color solid. LCMS (m/z): 193 (MH+), 0.35 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-d33774b115b54df3b8b879c9c18dabfe
Source noteuspto-grants-2016_01