HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755232Generated: October 26, 2026
Chloride → Methyl 6-(4-hydroxypiperidin-1-yl)pyridazine-3-carboxylate
https://huagongshe.com/reaction/1755232
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-chloropyridazine-3-carboxylic Acid | HCID 6415762 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 6-Methoxypyridazine-3-carboxylic acid | HCID 12214461 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 6-(4-hydroxypiperidin-1-yl)pyridazine-3-carboxylate | HCID 60980224 | 6,068.6% |
Reaction Steps
A solution of 6-chloropyridazine-3-carboxylic acid (0.50 g, 3.2 mmol) in 11 mL of SOCl2 was heated at 75° C. for 2 h and was then concentrated and redissolved in 5 mL of MeOH. To the solution was added a 25% solution of sodium methoxide (0.75 mL, 3.5 mmol, 1.1 eq) in MeOH. The reaction mixture was stirred at room temperature for 20 h and was then quenched with H2O and extracted with dichloromethane. Silica gel flash chromatography (EtOAc/MeOH 90:10) of the residue afford a 2:1 mixture of the 6-chloropyridazine-3-carboxylic acid and 6-methoxypyridazine-3-carboxylic acid (0.160 g). To a solution of the mixture of ester and chloride in 1.9 mL of p-dioxane was added 4-hydroxy piperidine (0.094 g, 93 mmol) followed by diisopropylethylamine (0.49 mL, 2.8 mmol). The mixture was heated at 100° C. for 20 h then concentrated. Purification with silica gel flash chromatography afforded methyl 6-(4-hydroxypiperidin-1-yl)pyridazine-3-carboxylate (0.15 g, 63 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169261B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-aee8372e6551426ba88f83a27e814aea |
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| Source note | uspto-grants-2015_10 |
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