Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820890생성일: 2026년 10월 26일
alpha-Chloro-m-nitrotoluene → 3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1820890
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine | HCID 11673285 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridine | HCID 57891754 | 77% |
반응 단계
3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1 (35 mg, 0.14 mmole) was dissolved in 15 mL of DMF and sodium hydride (60% dispersion in mineral oil, 10 mg, 0.25 mmol) was added in small portion to the reaction mixture. After stirring for 30 minutes, m-nitro-benzyl chloride (30 mg, 0.14 mmole) was added to the reaction mixture and was stirred for 2 hours. The reaction mixture was poured into 50 mL of ice water and was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate followed by saturated potassium bisulfate and then brine. The resulting solution was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate in hexanes) to yield 42 mg (71%) of the titled compound as a white solid. MS(ESI) [M+H+]+=390.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07605168B2 |
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| 출처 데이터셋 | uspto-grants-2009_10 |
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| ORD ID | ord-4ff113348dd74e3cac51b3bad10beb82 |
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| 출처 메모 | uspto-grants-2009_10 |
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