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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 724307Erstellt: 24. Oktober 2026

Triethylamine → HCID 178503227, Verbindung

https://huagongshe.com/de/reaction/724307

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt2-[3-(Methylsulfanyl)phenoxy]-5-fluoronicotinic acidHCID 11391823—
EduktHCID 178479277HCID 178479277—
LösungsmittelDimethylformamideHCID 6228—
ProduktAmmoniaHCID 222—
ProduktHCID 178503227HCID 178503227163,2%

Reaktionsschritte

5-Fluoro-2-(3-methylsulfanyl-phenoxy)-nicotinic acid (100 mg, 0.358 mmol) was dissolved in dimethylformamide (2 ml) and triethylamine (150 mg, 1.07 mmol) was added followed by cis-4-aminocyclohexanol hydrochloride (54 mg, 0.358 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (76 mg, 0.394 mmol) and 1-hydroxybenzotriazole (53 mg, 0.394 mmol). The reaction was stirred under nitrogen at room temperature for 18 h and the solvent was removed under reduced pressure. The residue was partitioned between sat. sodium bicarbonate solution (5 ml) and ethyl acetate (10 ml) and the aqueous phase was extracted with ethyl acetate (2×10 ml). The combined organic extracts were washed with water (2×3 ml), brine (3 ml), dried over MgSO4 and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel eluting with dichloromethane:methanol:concentrated aqueous ammonia (98:2:0.2, by volume) to give 5-fluoro-N-(cis-4-hydroxy-cyclohexyl)-2-(3-methylsulfanyl-phenoxy)-nicotinamide (110 mg) as a white foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07141586B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-e44cce910ed94f63a5f0be446c5579ca
Quellennotizuspto-grants-2006_11