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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167109Erstellt: 26. Oktober 2026

Methyl iodide → Methyl 2-methyl-2-phenyl-5-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-N-methyl-amino]-piperidin-1-yl}-pentanecarboxylate

https://huagongshe.com/reaction/1167109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktMethyl 2-methyl-2-phenyl-5-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylateHCID 22995529—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-methyl-2-phenyl-5-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-N-methyl-amino]-piperidin-1-yl}-pentanecarboxylateHCID 22995623—

Reaktionsschritte

0.095 g (0.803 mmol) of sodium hydride (55 to 65% in oil) are added to a solution of 0.4 g (0.724 mmol) of methyl 2-methyl-2-phenyl-5-{4-[(4′-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylate in 5 ml of dimethylformamide at ambient temperature and stirred for one hour. Then 0.05 ml (0.803 mmol) of methyl iodide are added and the mixture is stirred for 14 hours. The reaction solution is poured onto water, extracted with ethyl acetate, and the organic phase is dried over sodium sulphate. The product is purified by column chromatography on silica gel (eluant: dichloromethane/methanol=5:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617325B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-d437bc1c3c4347738e67317dc95dccbc
Quellennotizuspto-grants-2003_09