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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1269796Erstellt: 26. Oktober 2026

Cyclopentanol → 5-(cyclopentyloxy)-1H-indazole

https://huagongshe.com/reaction/1269796

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopentanolHCID 7298—
EduktTriphenylphosphineHCID 11776—
Edukt1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
Edukt1H-Indazol-5-olHCID 101438—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(cyclopentyloxy)-1H-indazoleHCID 2293392816%

Reaktionsschritte

Cyclopentanol (0.068 ml, 0.745 mmol), triphenylphosphine (221 mg, 0.820 mmol) and dibenzyl azodicarboxylate (267 mg, 0.895 mmol) were added at 0° C. to a solution of the 1H-indazol-5-ol (100 mg, 0.745 mmol) obtained in Reference Example 4 in tetrahydrofuran (6 ml). After 30 minutes, the mixture thus obtained was heated to room temperature. After stirring overnight, the reaction solution was concentrated under reduced pressure and a 1M-aqueous sodium hydroxide solution (4 ml) and chloroform (3 ml) were added to the resulting residue. After removing the aqueous layer, water (2 ml) was added to the residue. The aqueous layer was removed and the organic layer was dried over anhydrous magnesium sulfate. The organic layer dried was concentrated and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol, hexane/ethyl acetate) to obtain 5-(cyclopentyloxy)-1H-indazole (24 mg, 16%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07199147B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-7949bd9d092249aeaf3c59466e2055bd
Quellennotizuspto-grants-2007_04