HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715534Generated: October 27, 2026
Ethyl chloroformate → Ethyl (6-chloro-4-methylpyridazin-3-yl)carbamate
https://huagongshe.com/reaction/715534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 6-Chloro-4-methylpyridazin-3-amine | HCID 12353664 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl (6-chloro-4-methylpyridazin-3-yl)carbamate | HCID 86717594 | 58% |
Reaction Steps
A 100 mL flask was charged with 6-chloro-4-methylpyridazin-3-amine (700 mg, 4.88 mmol) and pyridine (20 mL) then ethyl chloroformate (0.421 mL, 4.39 mmol) was added portionwise. The reaction mixture was stirred for 1 h at 0° C. The reaction mixture was then concentrated and partitioned between ammonium chloride and DCM. The aqueous layer was extracted with DCM (2×). The organic layers were combined and washed with brine (1×), eluted through a phase separator and concentrated to afford ethyl (6-chloro-4-methylpyridazin-3-yl)carbamate (549 mg, 49.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187464B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-db37325d408a41d98a6fc68e47ca942b |
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| Source note | uspto-grants-2015_11 |
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