HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396418Generated: November 2, 2026
Acetone → Ethyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylate
https://huagongshe.com/reaction/1396418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 6-Propylpyridin-2-amine | HCID 3016309 | — |
| Reactant | Ethyl 4,6-dichloropyridazine-3-carboxylate | HCID 53428795 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylate | HCID 86689767 | 29% |
Reaction Steps
A mixture of ethyl 4,6-dichloropyridazine-3-carboxylate (0.80 g, 3.62 mmol) and 6-propylpyridin-2-amine (739 mg, 5.43 mmol) was dissolved in acetonitrile (4 mL) and heated at 130° C. After 24 h, the reaction mixture was cooled and concentrated in vacuo, then purified by chromatography (silica, 80 g, 0 to 3% acetone in dichloromethane over 15 min, then 3 to 10% acetone in dichloromethane over another 15 min) to give ethyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylate (335 mg, 1.04 mmol, 29%) as a pale yellow crystalline solid after drying under high vacuum at room temperature. LC-MS 321.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901124B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-ed07ed0d6e5f4ee49b15b055c433de28 |
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| Source note | uspto-grants-2014_12 |
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