HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69197Generated: October 27, 2026
Water → (Rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-quinolin-6-yl-ethanol
https://huagongshe.com/reaction/69197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone | HCID 86630275 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | (Rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-quinolin-6-yl-ethanol | HCID 87523391 | — |
Reaction Steps
(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-quinolin-6-yl-methanone (Stage 1.2, 500 mg, 1.62 mmol) was dissolved in anhydrous THF (10 mL) and cooled down to 0° C. Methylmagnesium bromide in toluene/THF (1.4 M, 1.27 mL) was slowly added and the RM was then warmed up to rt and stirred for 4 h. Water (2 mL) was added and the precipitate formed was filtered off. The filtrate was concentrated to give the title compound as a brown solid (tR 0.50 min (conditions 2), (MH+=325).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822468B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-689ce011c6a8432fa57aec440e4fb6a6 |
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| Source note | uspto-grants-2014_09 |
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