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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40384Generated: October 29, 2026

Methyl 2,2-difluoro-2-(quinolin-6-yl)acetate → HCID 57690938, compound

https://huagongshe.com/reaction/40384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2,2-difluoro-2-(quinolin-6-yl)acetateHCID 58955252—
Reactant1-(6-(3-Methylisoxazol-5-yl)pyridazin-3-yl)hydrazine hydrochlorideHCID 67502860—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 57690938HCID 57690938—

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of 1-(6-(3-methylisoxazol-5-yl)pyridazin-3-yl)hydrazine hydrochloride (200 mg, 879 μmol) and methyl 2,2-difluoro-2-(quinolin-6-yl)acetate (208 mg, 879 μmol) in 5 M HCl (1 mL) was appropriately sealed and heated to 150° C. with microwaves for 4 h. The reaction was then quenched by a dropwise into cold 5 M NaOH (2 mL) and aqueous extracted with CHCl3/IPA (25 mL). The organic phase was then dried over MgSO4, concentrated, and purified with silica (40 g) eluting with 1>5% 2 M NH3 in MeOH/DCM. The product was then further purified on RP-HPLC eluting with water/ACN (0.1% TFA). Combined fractions concentrated, dissolved in DCM (5 mL) and MeOH (5 mL), then stirred with Si-Carbonate (0.5 g; 35 mmol) for 1 h. Si-Carbonate removed by filtration and filtrated concentrated with <0.5 mL remaining with product isolated by trituration. MS (ESI pos. ion) m/z: 379 (MH+). Calc'd exact mass for C19H12F2N6O: 378.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-90d53261ef874e4ea3ff93899bda5202
Source noteuspto-grants-2013_09