Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260641생성일: 2026년 10월 25일
Sodium Iodide → [1-(2-Chloro-4-ethanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester
https://huagongshe.com/reaction/1260641
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | methyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetate | HCID 67218699 | — |
| 반응물 | 1-Bromomethyl-2-chloro-4-ethanesulfonyl-benzene | HCID 67219826 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [1-(2-Chloro-4-ethanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester | HCID 67219537 | — |
반응 단계
To an ice cooled (0° C.) stirred solution of (2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester ((2.68 g, 13.1 mmol) in dry DMF (95 ml) is added sodium hydride (577 mg of a 60% dispersion in mineral oil, 14.41 mmol). After stirring at room temperature for 1.5 hours, the reaction mixture is re-cooled to 0° C. and treated with 1-bromomethyl-2-chloro-4-ethanesulfonyl-benzene (6.6 g, 22.2 mmol) and sodium iodide (3.3 g, 22.2 mmol). The resulting mixture is stirred and allowed to warm to room temperature overnight. The reaction mixture is poured onto water (600 ml) and extracted with 1:1 ethyl acetate/diethyl ether (4×300 ml). The organic portions are washed with brine, dried (MgSO4) and concentrated in vacuo and the resulting crude is purified by chromatography on silica eluting with ethyl acetate/iso-hexane (1:8 increasing to 1:2) to yield the titled product. (MH+ 421)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08470848B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-0943b4dd7df54af2a12a73c866decbe3 |
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| 출처 메모 | uspto-grants-2013_06 |
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