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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 506502생성일: 2026년 10월 26일

Triethylamine → N-[6-(Pyrrolidin-1-yl)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/506502

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diethyl cyanophosphonateHCID 76257—
반응물6-(Pyrrolidin-1-yl)pyridin-3-amineHCID 3899172—
반응물5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431513—
용매DimethylformamideHCID 6228—
생성물N-[6-(Pyrrolidin-1-yl)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 2372863887%

반응 단계

0.28 ml (1.68 mmol) of diethyl cyanophosphonate is added, dropwise, at 20° C. under argon, to a solution of 0.402 g (1.4 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid (example 1.1) and of 0.274 g (1.68 mmol) of 3-amino-6-(pyrrolidin-1-yl)pyridine (WO 02/48152) in 10 ml of dry dimethylformamide. The mixture is stirred for ten minutes and then 0.43 ml (3.08 mmol) of triethylamine is added dropwise. The mixture is stirred at ambient temperature for 18 hours, concentrated under reduced pressure, and then taken up with 50 ml of ethyl acetate. This solution is then successfully washed with three times 20 ml of a saturated sodium hydrogen carbonate solution, 50 ml of water and 20 ml of a saturated sodium chloride solution, and then dried over sodium sulfate, filtered, and concentrated under reduced pressure. The solid obtained is triturated in isopropylether under hot conditions. 0.527 g of a solid is obtained, which solid is dried under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786104B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-bd461cec65f84b59837fa095b2b1d9a4
출처 메모uspto-grants-2010_08