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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875783생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/875783

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물1-[(4-methoxyphenyl)methyl]-1H-pyrazole-4-carboxylic acidHCID 43565362—
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)-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxamideHCID 6020547639.8%

반응 단계

A mixture of 5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (300 mg, 1.30 mmol, Example 1, Step H), 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylic acid (636 mg, 2.74 mmol), BOP-Cl (697 mg, 2.74 mmol), and triethylamine (0.909 mL, 6.52 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)-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxamide (230 mg, 39% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981085B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-97608d6f8ee64417b5ecad63dd3db4f0
출처 메모uspto-grants-2015_03