HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097306Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 25174777, compound
https://huagongshe.com/reaction/1097306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 25176544 | HCID 25176544 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium bicarbonate ethyl acetate | HCID 86584982 | — |
| Product | HCID 25174777 | HCID 25174777 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08143253B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-cca65224cc49420c88c169db4c865ead |
|---|
| Source note | uspto-grants-2012_03 |
|---|