HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863962Generated: October 25, 2026
5-Methylthiophene-2-carboxylic acid → 4-[3-(5-Methylthenoylamino)propylthio]pyridine
https://huagongshe.com/reaction/863962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Methylthiophene-2-carboxylic acid | HCID 74713 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 4-(3-Aminopropylthio)pyridine | HCID 15227695 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(5-Methylthenoylamino)propylthio]pyridine | HCID 19079238 | 64.5% |
Reaction Steps
To a solution of 1.27 g (8.91 mmol) of 5-methyl-2-thiophenecarboxylic acid and 1.33 g (11.6 mmol) of N-hydroxysuccinimide in 90 ml of methylene chloride, 2.05 g (10.7 mmol) of t-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 1 hour. Further, 1.50 g (8.91 mmol) of 4-(3-aminopropylthio)pyridine was added, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain powder. The powder thus obtained was washed with ether and dried to obtain 1.68 g of the desired compound (yield: 64.5%, colorless powder).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561147 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-1d2aa6f338be4994ac048c0e4b102156 |
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| Source note | uspto-grants-1996_10 |
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