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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907343Generated: October 27, 2026

Trifluoroacetic acid → (S)-6-(2-hydroxy-2-methylpropyl)-3-((S)-1-(imidazo[1,2-b]pyridazin-6-yl)piperidin-3-yl)-6-phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1907343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
Reactant(S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-piperidin-3-yl)-1,3-oxazinan-2-oneHCID 58278645—
SolventIsopropanolHCID 3776—
Product(S)-6-(2-hydroxy-2-methylpropyl)-3-((S)-1-(imidazo[1,2-b]pyridazin-6-yl)piperidin-3-yl)-6-phenyl-1,3-oxazinan-2-oneHCID 6674620810.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

The TFA salt of (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-piperidin-3-yl)-1,3-oxazinan-2-one (6 mg, 0.018 mmol), 6-chloroimidazo[1,2-b]pyridazine (6 mg, 2.15 equiv.), and i-Pr2NEt (30 μL, excess) were mixed with isopropanol (1 mL). The mixture was heated in a microwave oven at 160° C. for 2.5 h. After being cooled to rt, the mixture was filtered and purified by prep HPLC to afford the title compound (0.82 mg) as brown oil. LC-MS Method 1 tR=1.07 min., m/z=450 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598163B2
Source datasetuspto-grants-2013_12
ORD IDord-a811eb186a2a46718ff9d48ad087ce74
Source noteuspto-grants-2013_12