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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220601생성일: 2026년 10월 24일

Sodium Iodide → N-{4-[4-(1,5-Dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-benzyl}-N-methyl-acetamide hydrochloride

https://huagongshe.com/ko/reaction/220601

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물N-MethylacetamideHCID 6582—
반응물Sodium hydrideHCID 24758—
반응물3'-(4-chloromethyl-phenyl)-4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl dihydrochlorideHCID 68594160—
용매DimethylformamideHCID 6228—
생성물N-{4-[4-(1,5-Dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-benzyl}-N-methyl-acetamide hydrochlorideHCID 6859541029%

반응 단계

Dissolve N-methyl acetamide (187 mg, 2.55 mmol) in dry N,N-dimethylformamide (5 mL) at room temperature under nitrogen. Add sodium hydride (60% dispersion in oil, 102 mg, 2.55 mmol), stir for 1 hr., then add 3′-(4-chloromethyl-phenyl)-4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl dihydrochloride (300 mg, 0.64 mmol) and sodium iodide (96 mg, 0.64 mmol). Stir the reaction at 50° C. for 20 hr., the quench with water (10 mL). Extract with DCM (4×10 mL) and pass through an IST Phase Separator Frit®. Purify using SCX-2 chromatography, eluting with 3 M ammonia in methanol and further purify using silica gel chromatography (eluting with 5:95 methanol:DCM). Dissolve the clear oil in acetonitrile, and add 2 M aq. HCl and water then lyophilize to give the title compound as light yellow powder (87 mg, 29%). MS (ES): m/z=434 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202873B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-fde6d1702c7c484ca917001a3413a701
출처 메모uspto-grants-2012_06