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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053136Generated: October 30, 2026

Boron trifluoride etherate → 3-(1-Isopropyltriazol-4-yl)-5-[3-methoxy-4-(morpholinomethyl)phenyl]pyridin-2-amine

https://huagongshe.com/reaction/1053136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium borohydrideHCID 4311764—
Reactant[4-[6-Amino-5-(1-isopropyltriazol-4-yl)-3-pyridyl]-2-methoxy-phenyl]-morpholino-methanoneHCID 77106365—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Isopropyltriazol-4-yl)-5-[3-methoxy-4-(morpholinomethyl)phenyl]pyridin-2-amineHCID 7607357151.81%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of [4-[6-amino-5-(1-isopropyltriazol-4-yl)-3-pyridyl]-2-methoxy-phenyl]-morpholino-methanone (200 mg, 0.473 mmol) in THF (10.0 mL) was added BF3.Et2O (0.3 mL, 2.36 mmol) at 0° C. and stirred for 30 min. After 30 min, NaBH4 (89 mg, 2.36 mmol) was added at 0° C. and stirred at room temperature for 18 h. After cooling to 0° C., quenched with MeOH (2 mL) and heated to reflux for 6 h. The reaction mixture was diluted with EtOAc (50 mL), washed with water (30 mL), dried over anhydrous Na2SO4 and solvent was evaporated under reduced pressure. Crude compound was purified by column using 100-200 mesh silica gel. The column was eluted with 100% EtOAc to afford 100 mg (yield: 51.81%) of the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393248B1
Source datasetuspto-grants-2016_07
ORD IDord-136ac8fa10c3410bba8e1e9c0a4adf20
Source noteuspto-grants-2016_07