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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Methoxyethanimidamide hydrochloride | HCID 13548602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Methoxymethyl)-1,2,4-thiadiazol-5-amine | HCID 21688992 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-0a5cb7af2a87404d9ad64641dcf6e21a |
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| Source note | uspto-grants-2010_06 |
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