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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074342Generated: October 25, 2026

Triethylamine → Ethyl 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(cyclopropyloxyimino)acetate

https://huagongshe.com/reaction/1074342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantEthyl 2-amidino-2-(cyclopropyloxyimino)acetate hydrochlorideHCID 73867361—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(cyclopropyloxyimino)acetateHCID 5441862456.3%

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a solution of ethyl 2-amidino-2-(cyclopropoxyimino)acetate hydrochloride (syn isomer) (1.44 g) in methanol (11 ml) was added triethylamine (3.06 ml) at -15° C. To the solution was dropwise added bromine (852 mg) at -5° C. After the solution was stirred at -5° C. for 2 minutes, to the solution was added a solution of potassium thiocyanate (518 mg) in methanol (5 ml) at -5° C. The mixture was allowed to be stirred under ice-cooling for 2 hours. The mixture was concentrated in vacuo to give a residue. The residue was dissolved in ethyl acetate. The solution was washed successively with 1N hydrochloric acid, saturated aqueous solution of sodium bicarbonate, and saturated aqueous solution of sodium chloride, dried over magnesium sulfate, concentrated in vacuo, and triturated with diethyl ether to give ethyl 2-(5-amino-l,2,4-thiadiazol3-yl)-2-(cyclopropyloxyimino)acetate (syn isomer)(769 mg) as a crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973699
Source datasetuspto-grants-1990_11
ORD IDord-aca11c7722844dd38692216ba881e37e
Source noteuspto-grants-1990_11