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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19095Generated: October 29, 2026

Bromine → 3-(2-Methoxyethyl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/19095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Methoxypropanimidamide--hydrogen chloride (1/1)HCID 19847582—
SolventMethanolHCID 887—
Product3-(2-Methoxyethyl)-1,2,4-thiadiazol-5-amineHCID 6141254974%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 3-methoxy-propionamidine hydrochloride (4.8 g, 0.035 mol) in methanol (20 mL) at 0° C. under vigorous stirring was added dropwise bromine (1.78 mL, 0.035 mol) and a 5.4M sodium methylate solution in methanol (13 mL, 0.035 mol) simultaneously over 30 min maintaining a slight bromine excess by color. To the resulting nearly colorless suspension was added dropwise a solution of potassium thiocyanate (3.37 g, 0.035 mol) in methanol (20 mL) over 10 min at 0-10° C. The resulting mixture was stirred for 2 h at 0-10° C. and then filtered. The isolated material was washed with methanol and dried which afforded a brown solid which was purified by flash chromatography (300 g silica gel 60, 5% methanol/diethyl ether) and crystallized from diethyl ether/hexanes which afforded 3-(2-methoxy-ethyl)-[1,2,4]thiadiazol-5-ylamine (4.08 g, 74%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-1afbeec922e04669a0e78cb6788857f5
Source noteuspto-grants-2010_06