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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928438Generated: November 2, 2026

Potassium Carbonate → tert-butyl (5-((1-((7-chloroquinolin-2-yl)methyl)-1H-pyrazole-4-carboxamido)methyl)-4,6-dimethylpyridin-2-yl)carbamate

https://huagongshe.com/reaction/928438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-7-chloroquinolineHCID 10244160—
Reactanttert-Butyl 5-((1H-pyrazole-4-carboxamido)methyl)-4,6-dimethylpyridin-2-ylcarbamateHCID 58081315—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (5-((1-((7-chloroquinolin-2-yl)methyl)-1H-pyrazole-4-carboxamido)methyl)-4,6-dimethylpyridin-2-yl)carbamateHCID 58081351—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl (5-((1H-pyrazole-4-carboxamido)methyl)-4,6-dimethylpyridin-2-yl)carbamate (100 mg, 0.290 mmol) in acetone (2.5 ml) were added 2-(bromomethyl)-7-chloroquinoline (74.3 mg, 0.290 mmol) and K2CO3 (200 mg, 1.448 mmol). Reaction mixture was stirred for 5 h at 50° C. Reaction mixture was diluted with ethyl acetate and water. Phases were separated and organic layer was washed with brine, dried over sodium sulfate, filtered and evaporated to afford the title compound. HPLC (Method G) Rt=1.736 min, MS (Method V) [M+H]+=521.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290485B2
Source datasetuspto-grants-2016_03
ORD IDord-2b691995a27c41c5ba5e265ff44edb75
Source noteuspto-grants-2016_03