Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1700349Erstellt: 26. Oktober 2026

1-Hydroxybenzotriazole → 2-Cyanoethyl 4-(3-chlorophenyl)-2,6-dimethyl-5-{[3-(2-methoxyphenyl)-2-propene-1-yl]carbamoyl}-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1700349

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt3-(2-Methoxyphenyl)-allylamineHCID 3718721—
EduktMono(2-cyanoethyl) 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 86757801—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Cyanoethyl 4-(3-chlorophenyl)-2,6-dimethyl-5-{[3-(2-methoxyphenyl)-2-propene-1-yl]carbamoyl}-1,4-dihydropyridine-3-carboxylateHCID 70156792—

Reaktionsschritte

150 mg (0.416 mmol) of mono(2-cyanoethyl) 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate and 81.4 mg (0.499 mmol) of 3-(2-methoxyphenyl)-allylamine were dissolved in 10 ml of dichloromethane. 120 mg (0.624 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 63.7 mg (0.416 mmol) of 1-hydroxybenzotriazole were added to the obtained solution under cooling with ice, and they were stirred at room temperature for 2 hours. Dichloromethane was evaporated under reduced pressure. Ethyl acetate was added to the residue, and the product was washed with 1 N hydrochloric acid and then with a saturated aqueous sodium hydrogencarbonate solution. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (dichloromethane/methanol=100/1) to obtain the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06350762B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-a0f5701b66e2472a81e4804a782331ab
Quellennotizuspto-grants-2002_02