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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537494Generated: October 30, 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/537494

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 slica 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 numberUS08859591B2
Source datasetuspto-grants-2014_10
ORD IDord-3b2b80f1c7834ca5a5f5e8b59efffe49
Source noteuspto-grants-2014_10