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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1395894Erstellt: 27. Oktober 2026

Benzoyl chloride → 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/1395894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktTetrahydrofuranHCID 8028—
EduktDiisopropylethylamineHCID 81531—
Edukt3-(4-amino-benzyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 69447499—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 6945303783%

Reaktionsschritte

A solution of 3-(4-amino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (62 mg, 0.21 mmol), DIPEA (0.06 mL, 0.32 mmol), benzoyl chloride (0.03 mL, 0.23 mmol) and THF (5 mL) was stirred for 10 hr at room temperature. The solution was then diluted with ether (20 mL) and ethyl acetate (20 mL) and washed with aq. NaHCO3 (50 mL). The organic layer was dried over MgSO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane, 2:3) to provide 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (69 mg, 83% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08900565B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-6be7b1bf62cf47f2a2bab87b6ed634c7
Quellennotizuspto-grants-2014_12