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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064444Generated: November 2, 2026

1,2-Dichloroethane → HCID 57805514, compound

https://huagongshe.com/reaction/2064444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamateHCID 57805468—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57805514HCID 57805514—

Reaction Steps

To a round bottom flask was added EDC (4.63 g, 24.17 mmol), HOBt (3.27 g, 24.17 mmol), anhydrous DCM (50 mL) and acetic acid (13.2 mL, 13.86 mmol). The reaction mixture was then stirred at room temperature under an atmosphere of nitrogen for 30 minutes. Then added tert-butyl {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-6) (10.58 g, 21.97 mmol). The reaction mixture was then permitted to stir overnight (18 hours) at room temperature under an atmosphere of nitrogen, then heated to 80° C. for 2 hours. The reaction mixture was then suspended in ethyl acetate, slowly poured into a saturated solution of sodium bicarbonate, followed by water and brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue was purified by silica gel chromatography 1-20% IPA/DCM. The appropriate fractions were combined and the solvent was removed in vacuo to give tert-butyl {1-[4-(3-methyl-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl)phenyl]cyclobutyl}carbamate (1-6f) as a tan solid. MS (M+H)+: observed=506.2, calculated=506.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288407B2
Source datasetuspto-grants-2012_10
ORD IDord-d03e7aca0d4e4ff584081652b9b4f2d1
Source noteuspto-grants-2012_10