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HRID 1192076Erstellt: 26. Oktober 2026
Isopropylamine → 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-N-isopropyl-4-nitro-thiophene-2-carboxamide
https://huagongshe.com/reaction/1192076
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropylamine | HCID 6363 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 5-((3,5-Dichloropyridin-4-yl)thio)-4-nitrothiophene-2-carboxylic acid | HCID 60207317 | — |
| Edukt | Chloro-1,1,3,3-tetramethyluronium hexachloroantimonate | HCID 86664723 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-N-isopropyl-4-nitro-thiophene-2-carboxamide | HCID 46932422 | 57,9% |
Reaktionsschritte
Chloro-1,1,3,3-tetramethyluronium hexachloroantimonate (47 mg, 0.1 mmol) was added to a suspension of 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-4-nitro-thiophene-2-carboxylic acid (39 mg, 0.11 mmol) in dichloromethane (1 mL) and the mixture was stirred at ambient temperature for 10 min. A solution of isopropylamine (9 mg, 0.12 mmol) and triethylamine (12 mg, 0.12 mmol) in dichloromethane (0.5 mL) was added to the above mixture and was stirred at ambient temperature for over night. After passing through a ISOLUTE™ PE-AX cartridge to remove excess amines, the resulting mixture was concentrated and the residue was purified by reverse-phase HPLC to afford the title product as a white solid (25 mg, 49% yield). 1H NMR (300 MHz, d6-DMSO) δ: 9.0 (2H, s), 8.65 (1H, d), 8.50 (1H, s), 4.0 (1H, m), 1.25 (6H, d). MS m/z: 391.70, 393.80 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08680139B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-0c7ac7762bf64e229dcb91c43cb02e4a |
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| Quellennotiz | uspto-grants-2014_03 |
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