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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69205Generated: October 28, 2026

Iodine → HCID 57917487, compound

https://huagongshe.com/reaction/69205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPhosphinic AcidHCID 4124402—
Reactant(Rac)-1-[6-fluoro-2-(2-trimethylsilanyl-ethoxymethyl)-2h-indazol-5-yl]-1-[6-(1-methyl-1h-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-ethanolHCID 68631442—
Reactant(Rac)-1-[6-fluoro-1-(2-trimethylsilanyl-ethoxymethyl)-1h-indazol-5-yl]-1-[6-(1-methyl-1h-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-ethanolHCID 68640315—
SolventAcetic AcidHCID 176—
ProductHCID 57917487HCID 57917487—

Reaction Steps

A mixture of (rac)-1-[6-Fluoro-2-(2-trimethylsilanyl-ethoxymethyl)-2H-indazol-5-yl]-1-[6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-ethanol and (rac)-1-[6-Fluoro-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-yl]-1-[6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-ethanol (Stage 164.1, 563 mg, 1.109 mmol), iodine (844 mg, 3.33 mmol), H3PO2 (1.815 mL of a 50% aqueous solution, 16.64 mmol) and acetic acid (9.5 mL) were introduced in a microwave tube and the mixture was subjected to MW-irradiation at 150° C. for 5 min. The solvent was removed and the residue was taken up with 1 N HCl and washed with EtOAc three times. The aqueous layer was basified with NaOH pellets and extracted twice with EtOAc. The organics were joined and washed with brine, dried over Na2SO4 and the solvent was removed. The title compound was obtained as a racemic mixture (tR 1.0 min (conditions 2), MH+=362).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-2bef876e7a594495a363751dcba17381
Source noteuspto-grants-2014_09