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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-dimethyl-2-thioxo-2,3-dihydrobenzo[d]oxazole-6-carboxamideHCID 18967003—
Edukt1-[(3R)-pyrrolidin-3-yl]piperidine dihydrochlorideHCID 66905717—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelO-XyleneHCID 7237—
Produkt(R)-N,N-dimethyl-2-(3-(piperidin-1-yl)pyrrolidin-1-yl)benzo[d]oxazole-6-carboxamideHCID 44125449—

Reaktionsbedingungen

Temperatur150 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153813B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-06bcc887dc354e85b36daae3f60405b9
Quellennotizuspto-grants-2012_04