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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798931Generated: November 3, 2026

Acetic Acid → 2-Fluoro-4-methyl-6-{[1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinyl]amino}phenol

https://huagongshe.com/reaction/1798931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyano-borohydrideHCID 498716—
Reactant2-Amino-6-fluoro-4-methylphenolHCID 55282121—
Reactant1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinoneHCID 59683251—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-4-methyl-6-{[1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinyl]amino}phenolHCID 5828731446.5%

Reaction Steps

2-Amino-6-fluoro-4-methylphenol (D16, 49 mg, 0.34 mmol) was dissolved in DCM (3 mL) and 1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinone (D12, 68 mg, 0.34 mmol), polymer supported cyanoborohydride (160 mg, 0.69 mmol, 4.3 mmol/g) and acetic acid (0.10 mL, 1.72 mmol) were all added at room temperature. The mixture was reacted at 100° C. in the microwave for 10 min. The mixture was then cooled to room temperature, filtered and the solvent was removed under vacuum to give the crude product, an orange oil, which was purified via flash column chromatography (silica, DCM to 0.5% NH3/9.5% MeOH/90% DCM) to give 2-fluoro-4-methyl-6-{[1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinyl]amino}phenol (D17, 51 mg, 42%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344000B2
Source datasetuspto-grants-2013_01
ORD IDord-7c439d1ca1684e288645f75c87fb64af
Source noteuspto-grants-2013_01