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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434288생성일: 2026년 10월 26일

Hydrochloric Acid → 6-{2-{[4-(2-Cyclopropylaminoethoxy)benzyl]isopropylamino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/1434288

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium IodideHCID 4875—
반응물Cesium carbonateHCID 10796—
반응물Sodium HydroxideHCID 14798—
반응물2-chloro-N-cyclopropylacetamideHCID 735780—
반응물Borane;tetrahydrofuranHCID 2723981—
반응물Pivalic acid 6-{2-[(4-hydroxybenzoyl)isopropylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57933955—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-{2-{[4-(2-Cyclopropylaminoethoxy)benzyl]isopropylamino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793453037.1%

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온도60 °C

반응 단계

A mixture of pivalic acid 6-{2-[(4-hydroxybenzoyl)isopropylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (25 mg), 2-chloro-N-cyclopropylacetamide (13 mg), cesium carbonate (32 mg), potassium iodide (5.0 mg) and tetrahydrofuran (2 ml) was stirred for 5 hours at 60° C. To the reaction solution was added dropwise borane-tetrahydrofuran complex (1.0 M solution in tetrahydrofuran) (0.49 ml), and the solution was stirred at 60° C. for one day and one night. The reaction solution was cooled to room temperature, concentrated hydrochloric acid (0.08 ml) was added thereto, the solution was stirred for 1.5 hours at 60° C., then an aqueous solution of 5N sodium hydroxide (1 ml) was added thereto, and the solution was stirred for 8 hours at 60° C. The reaction solution was diluted with water, then extracted with ethyl acetate. The organic layer was concentrated under a nitrogen stream; purified from a solution of the resulting residue in N,N-dimethylformamide by LC-MS, the title compound (9.0 mg) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612114B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-9852d8dec263468eadf9219108ff44cb
출처 메모uspto-grants-2009_11