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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81950생성일: 2026년 10월 24일

2,6-Diethylaniline → 8-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

https://huagongshe.com/ko/reaction/81950

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DiethylanilineHCID 11369—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물potassium 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acidHCID 67076100—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물8-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 6707566370%

반응 단계

A suspension of potassium 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acid (180 mg, 0.73 mmol) in anhydrous dimethylformamide (5.0 mL) was treated with N-ethyl-N,N-diisopropylamine (0.258 mL, 1.47 mmol) and N-ethyl-N′,N′-diisopropyl carbodiimide hydrochloride (EDCI) (280 mg, 1.47 mmol) and 1-hydroxybenzotriazole (200 mg, 1.47 mmol). The mixture was then treated with 2,6-diethylaniline (0.170 mL, 1.1 mmol). The reaction was stirred at room temperature overnight. The reaction was diluted with water and the resulting precipitate was collected by filtration to afford the title compound (190 mg, 70% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846701B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e607a4f63824469db74a4ab864200bfa
출처 메모uspto-grants-2014_09