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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1188502생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → 4-Chloro-2-ethyl-1-{[5-(2-pyridinyl)-1,3,4-oxadiazol-2-yl]methyl}-1H-benzimidazole-5-carbonitrile

https://huagongshe.com/reaction/1188502

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물PicolinohydrazideHCID 255881—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(4-Chloro-5-cyano-2-ethyl-1H-benzimidazol-1-yl)acetic acidHCID 67404468—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-2-ethyl-1-{[5-(2-pyridinyl)-1,3,4-oxadiazol-2-yl]methyl}-1H-benzimidazole-5-carbonitrileHCID 6740498716.9%

반응 단계

(4-Chloro-5-cyano-2-ethyl-1H-benzimidazol-1-yl)acetic acid (0.017 g, 0.065 mmol) and EDCl (0.014 mg, 0.072 mmol) were combined in acetonitrile (3 mL) and stirred at rt for 3 min. 2-Pyridinecarbohydrazide (0.0094 g, 0.068 mmol) was added next and the resulting mixture was stirred for 60 min. To this solution was added THF (THF 3 mL) followed by tosyl chloride (0.015 g, 0.078 mmol) and P-BEMP (0.148 g, 0.325 mmol, 2.2 mmol/g resin load). The reaction vessel was sealed and heated to 100° C. in a microwave for 5 min. The resin was filtered away and washed with CH2Cl2 (×2). The concentrated filtrate was purified (SiO2, 25% EtOAc/hexanes) to afford the title compound (0.004 g): MS (APCI) m/z 365 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673948B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-f8598deb37e34b3a815dcb87c76c5e9c
출처 메모uspto-grants-2014_03