HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908187Generated: October 31, 2026
Methanesulfonic Acid → Methyl 3-(5-amino-1,3,4-thiadiazol-2-yl)propanoate
https://huagongshe.com/reaction/908187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Butanoic acid, 4-chloro-4-oxo-, methyl ester | HCID 73888 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-(5-amino-1,3,4-thiadiazol-2-yl)propanoate | HCID 54474128 | — |
Reaction Steps
3-Chlorocarbonyl-propionic acid methyl ester (4.4 g, 21 mmol) is added dropwise to a stirred suspension of thiosemicarbazide (4.0 g, 44 mmol) in THF (25 ml) at 0° C. After stirring at room temperature for 18 h the product which precipitates is removed by filtration and washed with diethyl ether. This product (7.1 g, 34 mmol) is suspended in toluene (30 ml) at 0° C. and methane sulfonic acid (3.37 ml, 52 mmol) is added dropwise to the stirred reaction. The reaction is heated at 70° C. for 3 hours then concentrated at reduced pressure. Methanol (30 ml) is added followed by slow addition of aqueous ammonia, with stirring, until the solution is basic. The titled compound which precipitates is removed by filtration and purified by chromatography on silica, eluting with chloroform-methanol (10:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017608B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-0a714bcfb4764588b3f0b05006714a1c |
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| Source note | uspto-grants-2011_09 |
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