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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942048Generated: October 26, 2026

Iodide Ion → (Rac)-6-[1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-ethyl]-5,7-difluoro-quinoline

https://huagongshe.com/reaction/1942048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodide IonHCID 30165—
ReactantPhosphinic AcidHCID 4124402—
Reactant(Rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(5,7-difluoro-quinolin-6-yl)-ethanolHCID 58147518—
SolventAcetic AcidHCID 176—
Product(Rac)-6-[1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-ethyl]-5,7-difluoro-quinolineHCID 58147541—

Reaction Steps

(rac)-1-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(5,7-difluoro-quinolin-6-yl)-ethanol (Intermediate D, 23.2 g, 63.7 mmol was dissolved in acetic acid (317 mL) and introduced in 23 microwave reactor-vials. Iodide (2.11 g×23, 191 mmol), followed by H3PO2 50% (2.28 mL×23, 464 mmol) were then added into each vial. Then they were submitted to microwave irradiations 5 min at 150° C. The combined RMs were concentrated in vacuo and the residue was diluted with water, basified by a 4 M NaOH solution and extracted with EtOAc (3×). The organics were joined and washed with brine, dried over Na2SO4 and the solvent was removed. The residue was triturated with diisopropyl ether. The precipitate formed was filtered off to give a beige solid (tR 3.60 min (conditions 1), tR 9.76/10.87 min (conditions 2), MH+=345, 1H-NMR in DMSO-d6: 8.93 (d, 1H); 8.43 (d, 1H); 8.16 (d, 1H); 7.93 (s, 1H); 7.67 (d, 1H); 7.58 (m, 1H); 7.25 (d, 1H); 5.06 (q, 1H); 1.88 (d, 3H)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389526B2
Source datasetuspto-grants-2013_03
ORD IDord-64fb8fc166294945b27a7d6b36a18ca1
Source noteuspto-grants-2013_03