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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2423928생성일: 2026년 10월 24일

Ammonia → 6-{2-{[4-(2-Dimethylaminoethoxy)-3-fluorobenzyl]isopropylamino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/ko/reaction/2423928

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Potassium IodideHCID 4875—
반응물Cesium carbonateHCID 10796—
반응물2-chloro-N,N-dimethylacetamideHCID 75886—
반응물Pivalic acid 6-{2-[(3-fluoro-4-hydroxybenzoyl)isopropylamino]-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934527—
반응물Lithium aluminum hydride-aluminum chlorideHCID 131727732—
용매TetrahydrofuranHCID 8028—
생성물6-{2-{[4-(2-Dimethylaminoethoxy)-3-fluorobenzyl]isopropylamino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793382838.3%

반응 단계

To cesium carbonate (36 mg) and potassium iodide (5.0 mg) were sequentially added a solution of pivalic acid 6-{2-[(3-fluoro-4-hydroxybenzoyl)isopropylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (25 mg) in tetrahydrofuran (0.8 ml) and a solution of 2-chloro-N,N-dimethylacetamide (11 mg) in tetrahydrofuran (0.2 ml), and the solution was stirred for 1.5 hours at 60° C. The reaction solution was let to cool, then lithium aluminum hydride-aluminum chloride (1.0 M solution in tetrahydrofuran) (0.57 ml) was added dropwise thereto followed by stirring for 1 hour at room temperature. Tetrahydrofuran and ammonia solution were sequentially added thereto, the solution was filtered through celite pad and concentrated under a nitrogen stream; purified from a solution of the resulting residue in N,N-dimethylformamide by LC-MS, the title compound (9.1 mg) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07960412B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-a42f54d9a6bd411f9e8b81ed5c057eb7
출처 메모uspto-grants-2011_06