Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920949Generated: October 29, 2026

Dichloromethane → HCID 86683167, compound

https://huagongshe.com/reaction/920949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-QuinolineethanolHCID 70532—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 86683166HCID 86683166—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86683167HCID 8668316776.5%

Reaction Steps

To 69.3 mg (0.264 mmol) in THF was added diisopropylazodicarboxylate (94 mg, 0.463 mmol) in THF under ice-cooling and under nitrogen. Then, the resulting solution was stirred for 30 min at room temperature to give a suspension. 8-Chloropyrido[4,3-d]pyridazin-1(2H)-one (24 mg, 0.132 mmol) in THF and then 2-(quinolin-2-yl)ethanol (22.89 mg, 0.132 mmol) in THF were added and the reaction mixture was stirred overnight at room temperature. The total amount of THF was 60 mL. Then, the reaction mixture was mixed with DCM and water. The organic phase was washed with 1N HCl and the organic phase was discharged. The aqueous phase was basified by 1N NaOH and extracted with DCM. The organic phase was dried and concentrated to give 34 mg (76%) of the title compound as bright beige solid. LC-MS: m/e 337.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273068B2
Source datasetuspto-grants-2016_03
ORD IDord-a0a766383f394fe3b2f066db993f536e
Source noteuspto-grants-2016_03