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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48571생성일: 2026년 10월 24일

Ethyl Acetate → 2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-N-indan-1-yl-2-phenyl-acetamide

https://huagongshe.com/ko/reaction/48571

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물DiisopropylethylamineHCID 81531—
반응물(+-)-1-AminoindanHCID 123445—
반응물PyBOPHCID 2724699—
반응물1-[(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-phenyl-acetic acidHCID 69758875—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-N-indan-1-yl-2-phenyl-acetamideHCID 2274283564%

반응 단계

To a solution of 1-[(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-phenyl-acetic acid (100 mg, 0.209 mmol) in 5 ml of dry DMF, were added PyBOP (109 mg, 0.209 mmol), 1-aminoindane (32.3 mg, 0.19 mmol) and dropwise diisopropylethylamine (Hünig's base). (75 μl, 0.437 mmol). The mixture reaction was stirred at RT under argon for 20 h. The mixture was then dissolved in CH2Cl2 and washed with water. The aqueous phase was extracted twice with CH2Cl2, the combined organic extracts were dried over MgSO4, filtered and concentrated to give a crude brown residue. Flash chromatography (AcOEt) gave 72 mg (64%) of the title compound as a pale brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703392B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-527294e8a58b45c3b7dcceae1de8be76
출처 메모uspto-grants-2004_03