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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2099979Erstellt: 27. Oktober 2026

Trichloroacetonitrile → 3-chloro-4-[(3,4-dimethoxyphenyl)methoxy]-N-methyl-N-[2-[[(1-methylethyl)amino]carbonyl]-4-phenoxyphenyl]-benzamide

https://huagongshe.com/reaction/2099979

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrichloroacetonitrileHCID 11011—
EduktTriphenylphosphineHCID 11776—
EduktN-isopropyl-2-(methylamino)-5-phenoxybenzamideHCID 57796896—
Edukt4-(3,4-Dimethoxybenzyloxy)-3-chlorobenzoic acidHCID 57796897—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-chloro-4-[(3,4-dimethoxyphenyl)methoxy]-N-methyl-N-[2-[[(1-methylethyl)amino]carbonyl]-4-phenoxyphenyl]-benzamideHCID 5779688887,7%

Reaktionsschritte

A slurry of 1B (28 mg, 0.09 mmol) and trichloroacetonitrile (0.009 mL, 0.09 mmol) in CH2Cl2 (1 mL) at room temperature was treated with a solution of triphenylphosphine (22 mg, 0.09 mmol) in THF (0.25 mL). The reaction mixture was stirred for 30 minutes and additional trichloroacetonitrile (0.009 mL, 0.09 mmol) and triphenylphosphine (22 mg, 0.09 mmol) were added. The resulting solution was treated with 44B (16 mg, 0.06 mmol) in CH2Cl2 (0.5 mL). The stirring was continued for 2 hours, and then the reaction concentrated to dryness. The residue was purified by chromatography (SiO2, 50% to 75% EtOAc in hexanes) to afford 44C (31 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07569725B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-2c90fc973cc74432bb313e260acb7af5
Quellennotizuspto-grants-2009_08