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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79553생성일: 2026년 10월 25일

3-bromo-4-chloro-5-phenyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine → 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-3-methyl-5-phenyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/79553

반응식

참여 물질

역할이름HCID투입량
반응물3-bromo-4-chloro-5-phenyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 68761431—
반응물HCID 178477797HCID 178477797—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물1H-Pyrrolo[2,3-b]pyridine, 4-chloro-3-methyl-5-phenyl-1-(phenylsulfonyl)-HCID 6876126287.8%

반응 조건

온도80 °C

반응 단계

Methyl zinc chloride (3.35 mL, 6.70 mmol) was added to 3-bromo-4-chloro-5-phenyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (1.00 g, 2.23 mmol) and Pd(PPh3)4 (0.129 g, 0.111 mmol) in THF (10 mL). The reaction was then heated to 80° C. for 2 hours, cooled to room temperature, and quenched with saturated NH4Cl. The resulting solids were filtered and discarded. The filtrate was diluted with DCM (500 mL) and was washed with water. The combined organic fractions were dried, filtered, and concentrated to give a crude solid that was purified by column chromatography (2:1 DCM:hexanes) to give 4-chloro-3-methyl-5-phenyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (0.75 g, 87.7% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841304B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-af45adbbb64e4ec3845891795d75ed55
출처 메모uspto-grants-2014_09