Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064432Generated: October 31, 2026

1,2-Dichloroethane → HCID 57805467, compound

https://huagongshe.com/reaction/2064432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-methyl-1H-imidazole-4-carboxylic acidHCID 541509—
ReactantTert-butyl {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamateHCID 57805468—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57805467HCID 57805467—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a round bottom flask was added tert-butyl {1-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-6) (3.94 g, 8.18 mmol), EDC (1.34 g, 10.6 mmol), HOBt (1.44 g, 10.6 mmol), 1-methyl-1H-imidazole-4-carboxylic acid (1.34 g, 10.6 mmol), and DMF (40 mL). The reaction mixture was heated to 60° C. while stirring under an atmosphere of nitrogen in a hot oil bath. After 45 minutes the reaction mixture was permitted to cool to room temperature, 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 to give tert-butyl {1-[4-(5-{2-[(1-methyl-1H-imidazol-4-yl)carbonyl]hydrazino}-3-phenyl-1,6-naphthyridin-2-yl)phenyl]cyclobutyl}carbamate (1-7) as red foam. MS (M+H)+: observed=590.3, calculated=590.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288407B2
Source datasetuspto-grants-2012_10
ORD IDord-9b5ee660103a4b1cad9dac688d71cf85
Source noteuspto-grants-2012_10