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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1644120생성일: 2026년 10월 27일

3-Furoic acid → (R)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide

https://huagongshe.com/reaction/1644120

반응식

참여 물질

역할이름HCID투입량
반응물3-Furoic acidHCID 10268—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Aminotetralin, (R)-HCID 7058072—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(R)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamideHCID 66772575—

반응 단계

To a solution of furan-3-carboxylic acid (100 mg, 0.68 mmol), HOBt (240 mg, 1.78 mmol) and EDCI.HCl (196 mg, 1.03 mmol) in CH2Cl2 (8 mL) and DMF (1.5 mL) at 0° C., was added (R)-1,2,3,4-tetrahydronaphthalen-1-amine (160 μL, 1.06 mmol). The reaction was stirred at rt for 24 h, after which CH2Cl2 was added. The resulting solution was washed with saturated NaHCO3, H2O, brine, dried over MgSO4 and concentrated in vacuo. Recrystallization from EtOH/H2O afforded (R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide. 1H NMR (500 MHz, CDCl3): δ 1.89 (m, 3H), 2.12 (m, 1H), 2.84 (m, 2H), 5.35 (m, 1H), 5.96 (br d, 1H, J=7.75 Hz), 6.59 (dd, 1H, J=1.90, 0.86 Hz), 7.13 (m, 1H), 7.19 (m, 2H), 7.32 (m, 1H), 7.43 (t, 1H, J=1.73 Hz), 7.93 (m, 1H). MS (M+H, 242).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124121B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-2f37b32b656749a18672abd29581afa3
출처 메모uspto-grants-2012_02