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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410277생성일: 2026년 10월 27일

Benzimidazole → Tert-butyl 4-(2-(4-(1H-benzo[D]imidazole-2-carbonyl)phenoxy)pyridin-3-YL)piperidine-1-carboxylate

https://huagongshe.com/reaction/410277

반응식

참여 물질

역할이름HCID투입량
반응물BenzimidazoleHCID 5798—
반응물Propane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
반응물Lithium diisopropylamideHCID 2724682—
반응물Tert-butyl 4-(2-(4-(ethoxycarbonyl)phenoxy)pyridin-3-YL)piperidine-1-carboxylateHCID 59326865—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(2-(4-(1H-benzo[D]imidazole-2-carbonyl)phenoxy)pyridin-3-YL)piperidine-1-carboxylateHCID 59326866—

반응 단계

A mixture of benzimidazole (0.351 g, 2.97 mmol) and triisopropyl orthoformate (3.9 mL, 17.61 mmol) in toluene (25 mL) was heated in a 100 mL round bottom flask equipped with a Dean-Stark trap and reflux condenser under an atmosphere of nitrogen. After 1 h the solvent was removed in vacuo. The residue was dissolved in THF (8 mL) and to the solution was added a solution of tert-butyl 4-(2-(4-(ethoxycarbonyl)phenoxy)pyridin-3-yl)piperidine-1-carboxylate (1.07 g, 2.509 mmol) in THF (8 mL). The mixture was cooled (−78° C.) and lithium diisopropylamide (2.0M solution in heptane/THF/ethylbenzene, 1.80 mL, 3.60 mmol) was added dropwise resulting in a reddish solution. After 2 h the reaction was quenched with saturated NH4Cl and allowed to warm to rt. The mixture was partitioned between EtOAc/saturated NaHCO3. The organic layer was washed with brine and dried over Na2SO4. The solution was filtered and the filtrate was evaporated onto silica gel and purified by flash chromatography (Isco, (120 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97) to give a white amorphous solid. MS (ESI, pos. ion) m/z: 499.1 (M+1). IC50 (uM) +++++.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759532B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-f47c03a2673a48b4b90c6879ad9a5605
출처 메모uspto-grants-2014_06