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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097306Generated: October 30, 2026

Diisobutylaluminum hydride → HCID 25174777, compound

https://huagongshe.com/reaction/1097306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 25176544HCID 25176544—
SolventDichloromethaneHCID 6344—
SolventSodium bicarbonate ethyl acetateHCID 86584982—
ProductHCID 25174777HCID 25174777—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3-[3-(2-Furan-3-yl-pyridin-4-yl)-imidazo[1,2-b]pyridazin-7-yl]-benzoic acid ethyl ester (Ex. 41) (1 eq, 0.122 mmol, 50 mg) is dissolved in DCM (1 ml) and the reaction mixture is cooled to −70° C. DIBAL-H (1.5 M in THF, 10 eq, 1.22 mmol, 1.74 ml) is then added and the reaction is stirred at this temperature for 3 h. The reaction mixture is then poured in NaHCO3/EtOAc. The organic phase is separated and the aqueous phase is extracted with EtOAc. The combined organic phases are washed with brine, dried over MgSO4, filtered and the solvent is removed in vacuo. The reaction mixture is purified by flash column chromatography eluting with 9:1 DCM/MeOH to afford {3-[3-(2-Furan-3-yl-pyridin-4-yl)-imidazo[1,2-b]pyridazin-7-yl]-phenyl}-methanol as a light brown solid; [M+H]+=369

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143253B2
Source datasetuspto-grants-2012_03
ORD IDord-cca65224cc49420c88c169db4c865ead
Source noteuspto-grants-2012_03