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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983416생성일: 2026년 10월 26일

Triethylamine → (1-Benzo[1,3]dioxol-5-yl-1,3,4,9-tetrahydro-beta-carbolin-2-yl)-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methanone

https://huagongshe.com/reaction/983416

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물1-(1,3-benzodioxol-5-yl)-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 201172—
반응물5-(3-(Trifluoromethyl)phenyl)-2-furoic acidHCID 688281—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(1-Benzo[1,3]dioxol-5-yl-1,3,4,9-tetrahydro-beta-carbolin-2-yl)-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methanoneHCID 12020635—

반응 단계

To a suspension of 5-(3-trifluoromethylphenyl)furoic acid (256 mg, 1 mmol) in DCM (20 mL, anhydrous) was added oxalyl chloride (165 mg, 1.3 mmol), followed by two drops of DMF. The mixture was stirred at room temperature for 1 h. A solution of 1-(3,4-methylenedioxyphenyl)-2,3,4,9-tetrahydro-1H-β-carboline (292 mg, 1 mmol) (prepared according to the process as disclosed in WO97/43287, Intermediate 7, page 24) and triethylamine (0.4 mL) in DCM (10 mL, anhydrous) was added and the mixture was stirred at room temperature for 16 h, washed sequentially with aqueous NaHCO3, brine (2×), 1N HCl and brine (2×) and dried with MgSO4. After evaporation of the solvent, a white solid was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06864253B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-3d91dc99fc354d4f99eb42b7ef3fbacb
출처 메모uspto-grants-2005_03