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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1244379Erstellt: 25. Oktober 2026

Boron trifluoride etherate → HCID 21919258, Verbindung

https://huagongshe.com/reaction/1244379

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
Edukt1-Benzyl-4,4-diethoxypiperidin-3-amineHCID 21729935—
Edukt4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboximidothioic acid methyl ester hydroiodideHCID 69184072—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 21919258HCID 219192581%

Reaktionsschritte

To a suspension of 0.04 g 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboximidothioic acid methyl ester hydroiodide in 1.8 ml tetrahydrofurane were added 0.1 g 1-benzyl-4,4-diethoxy-piperidin-3-ylamine in 1.8 ml tetrahydrofurane and the mixture was stirred at room temperature for 16 hours. Then 0.015 ml boron trifluoride etherate was added and the solvent was distilled off under vacuum. Again 0.015 ml boron trifluoride etherate was added and the mixture was dissolved in 1.5 ml dimethylformamide and heated for 15 minutes at 125° C. The solvent was distilled off and the residue was dissolved in dichloromethane and extracted with water. The organic layer was dried with sodium sulfate, filtered and the solvent was evaporated. Chromatography on silicagel with ethylacatate/heptane 1:1 to 2:1 yielded 0.4 mg (1%) 5-benzyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine as an amorphous solid; m/e=462 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07122545B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-11fac07d95c64a1cb1b38980ef5e47fc
Quellennotizuspto-grants-2006_10