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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875780생성일: 2026년 10월 25일

Triethylamine → N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-fluoro-4-methoxybenzamide

https://huagongshe.com/reaction/875780

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물3-Fluoro-4-methoxybenzoic acidHCID 2733401—
반응물5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amineHCID 60205276—
용매DichloromethaneHCID 6344—
생성물N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-fluoro-4-methoxybenzamideHCID 6020547290.2%

반응 단계

A mixture of 5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (200 mg, 0.87 mmol, Example 1, Step H), 3-fluoro-4-methoxybenzoic acid (311 mg, 1.83 mmol), BOP-Cl (0.465 g, 1.83 mmol), and triethylamine (0.606 mL, 4.35 mmol) in DCM (5 mL) was processed as described in Example 62, Step A, to provide N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-fluoro-4-methoxybenzamide (300 mg, 90% yield) as a solid. LCMS (APCI+) m/z 381.9, 383.9 (M+H)+, Retention time=3.23 minutes (Method 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981085B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-4d2d0c5449e148eb825b54f709627a2e
출처 메모uspto-grants-2015_03