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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1773958생성일: 2026년 10월 27일

trans-2-Phenylcyclopropanecarboxylic acid → (8-Bromo-5-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-((1R,2R)-2-phenyl-cyclopropyl)-methanone

https://huagongshe.com/reaction/1773958

반응식

참여 물질

역할이름HCID투입량
반응물trans-2-Phenylcyclopropanecarboxylic acidHCID 237413—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물8-Bromo-5-fluoro-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 89648457—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(8-Bromo-5-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-((1R,2R)-2-phenyl-cyclopropyl)-methanoneHCID 89648804—

반응 단계

A solution of 8-bromo-5-fluoro-1,2,3,4-tetrahydro-isoquinoline hydrochloride (200 mg, 0.75 mmol, 1.0 eq.) and the acid (1R,2R)-2-phenyl-cyclopropanecarboxylic acid (122 mg, 0.75 mmol, 1.0 eq.) in DMF (9 mL) was treated with 4-(dimethylamino)pyridine (367 mg, 3.00 mmol, 4.0 eq.) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (216 mg, 1.13 mmol, 1.5 eq.) and the resulting solution was stirred at r.t. for 18 hours. The reaction mixture was diluted with AcOEt (70 mL). The diluted solution was washed with 1N aq. HCl (3×30 mL), sat. aq. NaCl soln. (1×30 mL), dried over MgSO4, filtered, and concentrated in vacuo to give the desired compound as a pale yellow oil. The product was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09255090B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-4024b6914dc043e2b2e21d678db69627
출처 메모uspto-grants-2016_02