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HRID 1269796作成日:2026年10月26日

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

https://huagongshe.com/reaction/1269796

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentanolHCID 7298—
反応物TriphenylphosphineHCID 11776—
反応物1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
反応物1H-Indazol-5-olHCID 101438—
溶媒TetrahydrofuranHCID 8028—
生成物5-(cyclopentyloxy)-1H-indazoleHCID 2293392816%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199147B2
出典データセットuspto-grants-2007_04
ORD IDord-7949bd9d092249aeaf3c59466e2055bd
出典メモuspto-grants-2007_04