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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271218생성일: 2026년 10월 27일

Cesium carbonate → 2-Furancarboxamide, N-[2-methyl-4-(1-pyrrolidinyl)-7-quinazolinyl]-

https://huagongshe.com/reaction/1271218

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물FuramideHCID 69108—
반응물7-Bromo-2-methyl-4-pyrrolidin-1-yl-quinazolineHCID 22474939—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
생성물2-Furancarboxamide, N-[2-methyl-4-(1-pyrrolidinyl)-7-quinazolinyl]-HCID 997341922%

반응 단계

A suspension of 0.12 g (0.41 mmol) of 7-bromo-2-methyl-4-pyrrolidin-1-yl-quinazoline, 3.9 mg (0.021 mmol) of copper (I) iodide and 0.267 g (0.82 mmol) of caesium carbonate in dioxane (5 ml) was treated at RT under argon with 4.7 mg (0.041 mmol) of trans-1,2-diaminocyclohexane and 0.18 g (1.6 mmol) of 2-furamide and then heated at reflux under argon for 20 h. The reaction mixture was partitioned between EtOAc and water, the layers were separated, the organic layer washed twice with water dried over sodium sulphate and concentrated in vacuo. The residue was applied to silica gel column with CH2Cl2/MeOH/NH4OH (9:1:0.5) as eluent. Combination of the purified fractions and concentration in vacuo gave 29 mg (22%) of the furan-2-carboxylic acid (2-methyl-4-pyrrolidin-1-yl-quinazolin-7-yl)-amide as an off white solid. ISP mass spectrum, m/e: 323.4 (M+1 calculated for C18H18N4O2: 323).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205309B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-daf25bfb61484ba7bd434f4615e8a6ba
출처 메모uspto-grants-2007_04