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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398819Generated: October 27, 2026

Acetate → 6-Chloro-3-isothiocyanato-4-methylpyridazine

https://huagongshe.com/reaction/1398819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantWaterHCID 962—
ReactantThiophosgeneHCID 10040—
Reactant6-Chloro-4-methylpyridazin-3-amineHCID 12353664—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product6-Chloro-3-isothiocyanato-4-methylpyridazineHCID 866328738.2%

Reaction Steps

To a solution of 6-chloro-4-methylpyridazin-3-amine (2.86 g, 20.0 mmol) in aqueous sodium bicarbonate (10 mL) and tetrahydrofuran (40 mL) was added thiophosgene (1.69 mL, 22.0 mmol) dropwise at 0° C. After stirring for 1 hr, water and ethyl, acetate were added to the mixture and the insoluble materials were filtered off. The filtrate was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel eluting with a 10-50% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound (304 mg, 1.64 mmol, 8%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-a40b56ffdda44bd18a95220245db8f7f
Source noteuspto-grants-2014_12