HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127138Generated: October 25, 2026
Hydrochloric Acid → 2-acetamido-5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazole
https://huagongshe.com/reaction/127138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Pentanamine | HCID 12019 | — |
| Reactant | 5-(Acetylamino)-1,3,4-thiadiazole-2-sulfonyl chloride | HCID 12894451 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-acetamido-5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazole | HCID 20286099 | — |
Reaction Steps
1-Ethylpropylamine (0.1 mole) and water (50 ml) are charged into a glass reaction vessel fitted with a mechanical stirrer and thermometer. The solution is cooled to 20° C. and stirred while 2-acetamido-5-chlorosulfonyl-1,3,4-thiadiazole (0.1 mole) is added slowly while holding the reaction temperature between 0° C. and 20° C. At the conclusion of the addition, stirring is continued for a period of about 2 hours at room temperature. The reaction mixture is then neutralized with 6 N hydrochloric acid. Solids are filtered out, water washed and dried to yield the desired product 2-acetamido-5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255182 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-c43c42815bbb46be9f7e18a75cdefbf4 |
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| Source note | uspto-grants-1981_03 |
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