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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant6-Chloro-4-methylpyridazin-3-amineHCID 12353664—
SolventPyridineHCID 1049—
ProductEthyl (6-chloro-4-methylpyridazin-3-yl)carbamateHCID 8671759458%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187464B2
Source datasetuspto-grants-2015_11
ORD IDord-db37325d408a41d98a6fc68e47ca942b
Source noteuspto-grants-2015_11