돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 887467생성일: 2026년 10월 25일

Benzimidazole → 1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanone

https://huagongshe.com/reaction/887467

반응식

참여 물질

역할이름HCID투입량
반응물BenzimidazoleHCID 5798—
반응물Benzenesulfonic AcidHCID 7371—
반응물DiisopropylamineHCID 7912—
반응물Propane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
반응물Lithium diisopropylamideHCID 2724682—
반응물N-Methoxy-N-methyl-4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)benzamideHCID 59351159—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanoneHCID 59351128—

반응 조건

온도0 °C

반응 단계

A mixture of 1H-benzo[d]imidazole (0.039 g, 0.334 mmol), triisopropoxymethane (0.529 g, 2.78 mmol), benzenesulfonic acid (2.200 mg, 0.014 mmol) in toluene (5 mL) was heated at reflux for 3 h. The mixture was cooled, neutralized with diisopropylamine (0.1 ml), concentrated to dryness and diluted with 1 ml THF. The above solution was added to a stirred mixture of N-methoxy-N-methyl-4-(3-(tetrahydro-2H-thiopyran-4-yl)pyrazin-2-yloxy)benzamide (0.100 g, 0.278 mmol) in THF (3 mL). The resulting mixture was cooled to 0° C. and LDA (0.167 mL, 0.334 mmol) was added dropwise. The reaction mixture was stirred at RT overnight, quenched with saturated NH4Cl, extracted with EtOAc (3×), dried over MgSO4, concentrated and purified by ISCO (0-5% MeOH/DCM) to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 416.1 (M+1). IC50 (uM) +++++.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247418B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-e5504a42158c47bdb6081aed84d49f75
출처 메모uspto-grants-2012_08