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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69274Generated: October 29, 2026

Iodine → Trifluoroacetic acid

https://huagongshe.com/reaction/69274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPhosphinic AcidHCID 4124402—
Reactant1-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-2,2,2-trifluoro-1-(quinolin-6-yl)ethanolHCID 86635116—
SolventAcetic AcidHCID 176—
ProductTrifluoroacetic acidHCID 6422—
Product(Rac)-6-[1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-2,2,2-trifluoro-ethyl]-quinolineHCID 57917412—

Reaction Conditions

Temperature150 °C

Reaction Steps

Iodine (105 mg, 0.412 mmol) and H3PO2 (0.225 mL of a 50% aqueous solution, 2.059 mmol) were added to a solution of (rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-2,2,2-trifluoro-1-(quinolin-6-yl)ethanol (Stage 274.1, 52 mg, 0.137 mmol) in acetic acid (1.4 mL). The RM was heated at 150° C. for 45 min under microwave irradiations. The solvent was removed. The residue was taken up with EtOAc and extracted with 1N HCl twice. The combined aqueous layers was basified to pH 14 with NaOH pellets. It was then extracted with EtOAc/MeOH (9:1) twice. Combined organic layers was dried over Na2SO4, filtered and concentrated. After purification by preparative HPLC with acetonitrile and water (+0.1% TFA), the fraction containing the product was lyophilized to give a TFA salt of the title compound (tR 1.0 min (conditions 1), MH+=363).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-16d5f39b9bf445a0ad74045b040cd1ae
Source noteuspto-grants-2014_09