HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1882925Erstellt: 26. Oktober 2026
Phosgene → N-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamide
https://huagongshe.com/reaction/1882925
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosgene | HCID 6371 | — |
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Edukt | Quinoline | HCID 7047 | — |
| Edukt | 1-(Pyridin-4-yl)pyrrolidin-3-ol | HCID 21906198 | — |
| Edukt | 2-amino-N-(5-chloropyridin-2-yl)benzamide | HCID 21906381 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamide | HCID 21906357 | 32,8% |
Reaktionsschritte
To as solution of 1-(4-pyridinyl)-3-hydroxypyrrolidine (330 mg, 2.01 mmol) in dichloromethane (30 mL) was added methanesulfonic acid (0.15 mL, 2.31 mmol). After 15 seconds, quinoline (0.3 mL, 2.54 mmol) was added, immediately followed by a toluene solution of phosgene (0.65 mL, 1.25 mmol). After 5 minutes, the reaction was placed in an oil bath at 35° C. After 45 minutes, the r action was cooled to room temperature. N-(5-Chloro-pyridin-2-yl)-2-aminobenzamide (498 mg, 2.01 mmol) was added, followed by quinolin (0.3 mL, 2.54 =mmol). After stirring overnight, the reaction was diluted with dichloromethane (150 mL) and washed with saturated aqueous sodium carbonate (2×25 mL). The organic layer was concentrated in vacuo and purified by flash column chromatography (100% CH2Cl2 to 9% MeOH/CH2Cl2) and then by HPLC to give the title product (181 mg, 0.41 mmol, 21%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06759414B2 |
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| Quelldatensatz | uspto-grants-2004_07 |
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| ORD ID | ord-c9daee0915b54de680f8ee8a672f60d7 |
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| Quellennotiz | uspto-grants-2004_07 |
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