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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798928Generated: October 31, 2026

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

https://huagongshe.com/reaction/1798928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Amino-4-(trifluoromethyl)phenolHCID 120246—
ReactantCyano-borohydrideHCID 498716—
Reactant1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinoneHCID 59683251—
SolventDichloromethaneHCID 6344—
Product2-{[1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinyl]amino}-4-(trifluoromethyl)phenolHCID 5828730760%

Reaction Conditions

Temperature100 °C

Reaction Steps

Polymer supported cyanoborohydride (191 mg, 0.82 mmol) was added to a solution of 1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinone (D12, 87 mg, 0.44 mmol), 2-amino-4-(trifluoromethyl)phenol (D7, 74 mg, 0.42 mmol, 4.3 mmol/g) and acetic acid (0.12 mL, 2.09 mmol) in DCM (2.5 mL). The mixture was heated by microwave at 100° C. for 10 min before being filtered and concentrated by rotary evaporation to give a yellow oil, which was purified via flash column chromatography (silica, DCM to 0.5% NH3/9.5% MeOH/90% DCM) to give 2-{[1-(4-methyltetrahydro-2H-pyran-4-yl)-4-piperidinyl]amino}-4-(trifluoromethyl)phenol (D14, 89 mg, 60%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344000B2
Source datasetuspto-grants-2013_01
ORD IDord-75ae5d5d1f0c4c4186c35236c1d7e7f6
Source noteuspto-grants-2013_01