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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892708Generated: October 31, 2026

6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amine → (+/-)-methyl 4-((tetrahydro-2H-pyran-4-yl)((6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-yl)amino)methyl)benzoate

https://huagongshe.com/reaction/1892708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amineHCID 64173296—
Reactantmethyl 4-(tetrahydro-2H-pyran-4-carbonyl)benzoateHCID 68156933—
ReactantHCID 178419135HCID 178419135—
SolventMethanolHCID 887—
Product(+/-)-methyl 4-((tetrahydro-2H-pyran-4-yl)((6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-yl)amino)methyl)benzoateHCID 6815680678%

Reaction Steps

A round bottom flask was charged with methyl 4-(tetrahydro-2H-pyran-4-carbonyl)benzoate (150 mg, 572 mmol), 6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amine (130 mg, 572 mmol) and MeOH (1.2 mL). Decaborane reagent (26.4 mg, 229 mmol) was added in one portion and the reaction stirred over the week-end. The reaction mixture was quenched with HCl solution (1N, aq.) and extracted with EtOAc twice. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Purification by silica gel flash chromatography (ethyl acetate/heptane) provide (±)-methyl 4-((tetrahydro-2H-pyran-4-yl)((6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-yl)amino)methyl)benzoate (206 mg, 78%) as a colorless gum. MS (M+1): 461.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507533B2
Source datasetuspto-grants-2013_08
ORD IDord-e0fbd3cd1ec4425292f5b6aed9544135
Source noteuspto-grants-2013_08