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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1628671생성일: 2026년 10월 26일

Ammonium Chloride → 1-[1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl]-N,N-dimethylmethanamine

https://huagongshe.com/reaction/1628671

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참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Borane-tetrahydrofuranHCID 11062302—
반응물1-(2,4-Dichlorophenyl)-N,N-dimethyl-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxamideHCID 57785961—
생성물1-[1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl]-N,N-dimethylmethanamineHCID 5778608628.5%

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온도70 °C

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To a solution of 1-(2,4-dichlorophenyl)-N,N-dimethyl-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxamide (200 mg, 0.513 mmol) was added boron-tetrahydrofuran complex (1.0 M solution in tetrahydrofuran, 2.6 mL, 2.6 mmol), and the mixture was stirred at 70° C. for 13 hr. To the mixture was added aqueous saturated ammonium chloride, and the mixture was stirred at 70° C. for 20 main. The mixture was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 50-100% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the solid, which was washed with diisopropyl ether to give the title compound as a colorless powder (54.8 mg, 0.146 mmol, 28%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785460B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-6f4fd756a7cf4f42819b603bb42179b1
출처 메모uspto-grants-2014_07