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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19107Generated: October 25, 2026

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

https://huagongshe.com/reaction/19107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Methoxyethanimidamide hydrochlorideHCID 13548602—
SolventMethanolHCID 887—
Product3-(Methoxymethyl)-1,2,4-thiadiazol-5-amineHCID 2168899260.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 2-methoxy-acetamidine hydrochloride (4.66 g, 0.037 mol) in methanol (20 mL) at 0° C. under vigorous stirring was added dropwise bromine (1.90 mL, 0.037 mol) and a 5.4M sodium methylate solution in methanol (13.7 mL, 0.037 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 (3.64 g, 0.037 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 filtered. The isolated material was washed with methanol and dried which afforded a brown solid which was purified by flash chromatography (silica gel 60, 5% methanol/diethyl ether) and crystallized from diethyl ether/hexanes which afforded 3-methoxymethyl-[1,2,4]thiadiazol-5-ylamine (3.25 g, 60%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-0a5cb7af2a87404d9ad64641dcf6e21a
Source noteuspto-grants-2010_06