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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410297생성일: 2026년 10월 26일

Cerium(III) chloride → 3-(2-(4-((1H-Benzo[D]imidazol-2-YL)(hydroxy)methyl)phenoxy)pyridin-3-YL)cyclopent-2-enol

https://huagongshe.com/reaction/410297

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참여 물질

역할이름HCID투입량
반응물Cerium(III) chlorideHCID 24636—
반응물VertellusHCID 22959485—
반응물3-(2-(4-(1H-Benzo[D]imidazole-2-carbonyl)phenoxy)pyridin-3-YL)cyclopent-2-enoneHCID 46214872—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물3-(2-(4-((1H-Benzo[D]imidazol-2-YL)(hydroxy)methyl)phenoxy)pyridin-3-YL)cyclopent-2-enolHCID 59326790—

반응 조건

온도0 °C

반응 단계

A suspension of 3-(2-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyridin-3-yl)cyclopent-2-enone (2125 mg, 5.37 mmol) and cerium (iii) chloride (1325 mg, 5.37 mmol) in tetrahydrofuran (300 mL) and methanol (30.0 mL) was cooled to 0° C. under nitrogen. Sodium borohydrate (813 mg, 21.50 mmol) was added in 4 lots over 20 min. The reaction was warmed to 23° C. over 2 h. After a total reaction time of 4 h, the reaction was quenched with saturated ammonium chloride solution (10 ml, slowly—effervescence). The solution was diluted with EtOAc (500 mL) and washed with saturated ammonium chloride solution (100 mL) and brine (100 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluant: 1-8% methanol/dichloromethane), affording the product as a yellow film.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759532B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-1e7816eab4f94e2db15a1379ce9bb402
출처 메모uspto-grants-2014_06