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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29297생성일: 2026년 10월 26일

Cesium carbonate → 4-(Cyclopropanecarbonyl-amino)-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/29297

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물CyclopropanecarboxamideHCID 80376—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl esterHCID 86599026—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물4-(Cyclopropanecarbonyl-amino)-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6871608298%

반응 단계

To 3-methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl ester (300 mg, 0.85 mmol, 1 eq, prepared according to Example 20, Step 1) in 8 mL of dioxane under nitrogen were added cyclopropyl carboxamide (87 mg, 1.02 mmol, 1.2 eq), Pd2 (dba)3 (16 mg, 0.017 mmol, 0.02 eq), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (30 mg, 0.051 mmol, 0.06 eq), and cesium carbonate (390 mg, 1.19 mmol, 1.4 eq). The reaction mixture was heated at reflux for 72 h. After work up and column chromatography (dichloromethane/hexanes), 4-(cyclopropanecarbonyl-amino)-3-methyl-benzofuran-2-carboxylic acid ethyl ester was obtained in 98% yield (238 mg). 1H NMR (400 MHz, DMSO-d6) δ ppm 0.8 (m, 4 H) 1.3 (t, J=7.1 Hz, 3 H) 1.8 (s, 1 H) 2.6 (s, 3 H) 4.4 (q, J=7.2 Hz, 2 H) 7.2 (d, J=7.1 Hz, 1 H) 7.5 (m, 1 H) 7.5 (m, 1 H) 10.1 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-6cb6a804429c49f08029e7b531d8aa19
출처 메모uspto-grants-2008_09