HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1692031Erstellt: 26. Oktober 2026
N,N-dimethyl-2-thioxo-2,3-dihydrobenzo[d]oxazole-6-carboxamide → (R)-N,N-dimethyl-2-(3-(piperidin-1-yl)pyrrolidin-1-yl)benzo[d]oxazole-6-carboxamide
https://huagongshe.com/reaction/1692031
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N-dimethyl-2-thioxo-2,3-dihydrobenzo[d]oxazole-6-carboxamide | HCID 18967003 | — |
| Edukt | 1-[(3R)-pyrrolidin-3-yl]piperidine dihydrochloride | HCID 66905717 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | (R)-N,N-dimethyl-2-(3-(piperidin-1-yl)pyrrolidin-1-yl)benzo[d]oxazole-6-carboxamide | HCID 44125449 | — |
Reaktionsschritte
N,N-Dimethyl-2-thioxo-2,3-dihydrobenzo[d]oxazole-6-carboxamide (Example 92C, 44 mg, 0.119 mmol) and (R)-1-(pyrrolidin-3-yl)piperidine dihydrochloride (Reference Example 5c, 54 mg, 0.238 mmol) were combined in xylene (1 mL) and heated to 150° C. for 30 minutes. The mixture was diluted with dichloromethane, washed with water, and the organic layer was absorbed on silica gel. The crude mixture was purified by silica gel chromatography eluting with a gradient of methanol in dichloromethane (2-20%) to afford the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.43-1.53 (m, 2 H) 1.59-1.70 (m, 4 H) 1.91-2.07 (m, 1 H) 2.23-2.35 (m, 1 H) 2.40-2.62 (m, 4 H) 2.93-3.13 (m, 7 H) 3.41-3.51 (m, 1 H) 3.55-3.66 (m, 1 H) 3.80-3.90 (m, 1 H) 3.96 (dd, J=10.00, 7.29 Hz, 1 H) 7.22-7.28 (m, 1 H) 7.30-7.35 (m, 1 H) 7.37-7.40 (m, 1 H); MS (ESI+) m/z 343.0 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08153813B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-06bcc887dc354e85b36daae3f60405b9 |
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| Quellennotiz | uspto-grants-2012_04 |
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