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HRID 392157Erstellt: 24. Oktober 2026

Benzo[b]thiophene-3-ethanamine → HCID 10045921, Verbindung

https://huagongshe.com/de/reaction/392157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzo[b]thiophene-3-ethanamineHCID 26743—
EduktSodium BicarbonateHCID 516892—
Edukt[(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl4-bromobenzenesulfonateHCID 20624762—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktHCID 10045921HCID 10045921—

Reaktionsschritte

To a stirred solution of 2-benzo[b]thiophen-3yl-ethylamine (354 mg, 2.0 mmol) in 1 mL of anhydrous DMSO was added [(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl 4-bromo-benzenesulfonate (300 mg, 0.67 mmol). The reaction mixture was stirred at ambient temperature for 4 days. The reaction was diluted with H2O (10 mL), poured into saturated aqueous sodium bicarbonate (25 mL) and extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with 1:1 H2O/brine (40 mL) and brine (40 mL), then were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuum. Flash chromatography (2×20 cm SiO2, CH2Cl2 to 3% MeOH/CH2Cl2 gradient) afforded 225 mg (86%) of the (S)-enantiomer of the title compound as a thick oil. The fumarate salt was prepared by treating the amine in ethyl acetate with a solution of 66 mg (0.57 mmol) fumaric acid in methanol. The precipitated salt, a pale yellow solid, weighed 190 mg (m.p. 124-127° C.); MS (ESI) m/z 391 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06800637B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-e5563d0d581b4f80ac23250d52eef666
Quellennotizuspto-grants-2004_10