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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42369Generated: October 29, 2026

Dimethylformamide → HCID 58216598, compound

https://huagongshe.com/reaction/42369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamateHCID 57805516—
Reactanttert-Butyl (6-chloro-2-formylpyridin-3-yl)carbamateHCID 58216578—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 58216598HCID 58216598—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a round bottom flask was added tert-butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate (1-3) (2.7 g, 6.1 mmol), tert-butyl (6-chloro-2-formylpyridin-3-yl)carbamate (1-4) (1.6 g, 6.1 mmol), potassium carbonate (5.0 g, 6.0 mmol), and DMF (20 mL). The reaction mixture was heated to 80° C. while stirring in a hot oil bath under an atmosphere of nitrogen for 15 hours. Then the reaction mixture was warmed to 120° C. for 1 hour. The reaction mixture was permitted to cool to room temperature, added water, suspended in ethyl acetate, washed with a saturated solution of sodium bicarbonate, followed by water, brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (5-50% EtOAc/5% DCM/Hexane) to give tert-butyl {1-[4-(6-chloro-3-phenyl-1,5-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-5) as an off-white solid. HRMS (M+H)+: observed=486.1954, calculated=486.1943.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536193B2
Source datasetuspto-grants-2013_09
ORD IDord-cb2a375574994237b62a87a93fcd5f83
Source noteuspto-grants-2013_09