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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104126Generated: October 31, 2026

1,2-Dichloroethane → HCID 57805489, compound

https://huagongshe.com/reaction/2104126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
ReactantTert-butyl {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamateHCID 57805468—
ProductHCID 57805489HCID 57805489—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a microwave vial was added {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-6) (51.2 mg, 0.106 mmol), EDC (102 mg, 0.532 mmol) and DMF (0.6 mL). The reaction mixture was heated under microwave irradiation for 5 minutes at 80° C. (high absorption). Acetic acid (0.5 mL) was added and the reaction mixture was heated under microwave irradiation for 5 minutes at 80° C. (high absorption), The resulting residue was purified by reverse phase column chromatography (Sunfire C18) eluting with 5 to 95% acetonitrile/(0.1% TFA/water) gradient. The appropriate fractions were free based by suspending in ethyl acetate, washed with a saturated solution of sodium bicarbonate, followed by water, brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give tert-butyl (1-{4-[3-(ethylamino)-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl]phenyl}cyclobutyl)carbamate (3-1) as an off-white solid. HRMS (M+H)+: observed=535.2800, calculated=535.2816.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576209B2
Source datasetuspto-grants-2009_08
ORD IDord-ece1fa2298db4c0fb22bfea8926dc9ea
Source noteuspto-grants-2009_08