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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269796생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1269796

반응식

참여 물질

역할이름HCID투입량
반응물CyclopentanolHCID 7298—
반응물TriphenylphosphineHCID 11776—
반응물1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
반응물1H-Indazol-5-olHCID 101438—
용매TetrahydrofuranHCID 8028—
생성물5-(cyclopentyloxy)-1H-indazoleHCID 2293392816%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199147B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-7949bd9d092249aeaf3c59466e2055bd
출처 메모uspto-grants-2007_04