HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639576Generated: November 2, 2026
Hydrogen Sulfide → 2-(3-Methyl-[1,2,4]thiadiazol-5-yl)-7-thiocarbamoyl heptanoic acid phenylamide
https://huagongshe.com/reaction/1639576
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | 7-Cyano-2-(3-methyl[1,2,4]thiadiazol-5-yl)heptanoic acid phenylamide | HCID 59378058 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | 2-(3-Methyl-[1,2,4]thiadiazol-5-yl)-7-thiocarbamoyl heptanoic acid phenylamide | HCID 59378072 | — |
Reaction Steps
To a stirred mixture of 7-cyano-2-(3-methyl[1,2,4]thiadiazol-5-yl)heptanoic acid phenylamide (2021044) (0.55 g, 1.7 mmol) in pyridine (120 mL) and piperidine (30 mL) was slowly bubbled hydrogen sulphide for 15 min. The resultant mixture was then stoppered and stirred at 50° C. for five days. The solvent was removed under reduced pressure, water (150 mL) was added to the residue, and the resultant solution was extracted with dichloromethane (3×150 mL). The crude product (1.6 g) was purified by preparative liquid chromatography to afford 2-(3-methyl-[1,2,4]thiadiazol-5-yl)-7-thiocarbamoyl heptanoic acid phenylamide (2021036) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110577B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-ddac096b9cb94c1fa2d88ed8f63b202b |
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| Source note | uspto-grants-2012_02 |
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