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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820891생성일: 2026년 10월 27일

N,N-Diethyl-2-propanamine → [3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-4-nitro-phenyl)-methanone

https://huagongshe.com/reaction/1820891

반응식

참여 물질

역할이름HCID투입량
반응물N,N-Diethyl-2-propanamineHCID 521913—
반응물PyBroPHCID 2733179—
반응물2-Ethoxy-4-nitrobenzoic acidHCID 2736347—
반응물3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
용매DichloromethaneHCID 6344—
생성물[3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-4-nitro-phenyl)-methanoneHCID 5789170277.5%

반응 단계

3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1(250 mg, 0.98 mmole) was dissolved in 50 mL of CH2Cl2. N,N-diethylisopropylamine (205 uL, 1.2 mmol), 2-ethoxy-4-nitro-benzoic acid (228 mg, 1.1 mmol) and bromotris(pyrolodino)phoshonium hexafluorophosphate (550 mg, 1.1 mmol) were added to the stirring reaction mixture. The mixture was stirred at ambient temperature for 4 h and washed consecutively with saturated sodium bicarbonate and saturated potassium bisulfate solution. The resulting solution was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate in hexanes) to yield 340 mg (77%) of the titled compound as a yellow solid. MS(ESI) [M+H+]+=448.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07605168B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-3a8ccfd22a4e4c6b98e6fdbdda52c2a2
출처 메모uspto-grants-2009_10