Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555880생성일: 2026년 10월 26일
Benzimidazole → 1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanone
https://huagongshe.com/reaction/555880
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzimidazole | HCID 5798 | — |
| 반응물 | Benzenesulfonic Acid | HCID 7371 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Propane, 2,2',2''-[methylidynetris(oxy)]tris- | HCID 78191 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | N-Methoxy-N-methyl-4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)benzamide | HCID 59351159 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanone | HCID 59351128 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08053438B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-7f607c30c0094b30b3f5737be1cda2ec |
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| 출처 메모 | uspto-grants-2011_11 |
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