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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1433585Erstellt: 26. Oktober 2026

1-Hydroxybenzotriazole → 4-Chloro-2-[(cyclopropylmethyl)aminocarbonyl]pyridine

https://huagongshe.com/reaction/1433585

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt(Cyclopropylmethyl)ammonium chlorideHCID 81671—
Edukt4-Chloropyridine-2-carboxylic acidHCID 230890—
Edukt1-(3-Diethylaminopropyl)-3-ethylcarbodiimide hydrochlorideHCID 9964512—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
Produkt4-Chloro-2-[(cyclopropylmethyl)aminocarbonyl]pyridineHCID 34829121—

Reaktionsschritte

4-Chloro-2-carboxypyridine (2.0 g), (aminomethyl)cyclopropane hydrochloride (1.7 g), 1-ethyl-3-(3-diethylaminopropyl)carbodiimide hydrochloride (WSC) (2.9 g), 1-hydroxybenzotriazole (HOBt) (2.3 g), triethylamine (2.1 ml) and tetrahydrofuran (30 ml) were stirred together at room temperature for 2 hours. Water was added, extraction was performed with ethyl acetate, and then silica gel was added to the extract and the solvent was distilled off under reduced pressure. The silica gel was charged into a dry column packed with silica gel and purified by column chromatography (hexane:ethyl acetate=4:1, followed by 2:1) to obtain 1.5 mg of the target substance as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612092B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-d4be9d575dae478c84c8674a87194404
Quellennotizuspto-grants-2009_11