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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1034781생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1034781

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 번호US08545897B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-acf77ddcbd8d4c42b6dc61f9251e2166
출처 메모uspto-grants-2013_10