HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 988596Erstellt: 23. Oktober 2026
Phosgene → N-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamide
https://huagongshe.com/de/reaction/988596
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 reaction was cooled to room temperature. N-(5-Chloropyridin-2-yl)-2-aminobenzamide (498 mg, 2.01 mmol) was added, followed by quinoline (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 | US06635657B1 |
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| Quelldatensatz | uspto-grants-2003_10 |
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| ORD ID | ord-57330204374a45c9a659e73a357b3a1b |
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| Quellennotiz | uspto-grants-2003_10 |
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