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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1399121생성일: 2026년 10월 26일

Triethylamine → 1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amine

https://huagongshe.com/reaction/1399121

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diphenylphosphinic acidHCID 15567—
반응물1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylic acidHCID 57786403—
용매tert-ButanolHCID 6386—
생성물1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amineHCID 57786170—

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온도90 °C

반응 단계

A mixture of 1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylic acid (9.40 g, 25.9 mmol), diphenylphosphinic acid (7.85 g, 28.5 mmol) and triethylamine (4.0 mL) in t-butanol (250 mL) was stirred at 90° C. for 12 hr and concentrated in vacuo. A mixture of the residue and trifluoroacetic acid (100 mL) in dichloromethane (50 mL) was stirred at room temperature for 20 hr and concentrated in vacuo. The residue was diluted with saturated aqueous sodium hydrogen carbonate and 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 10-60% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a yellow amorphous (440 mg, 1.32 mmol, 5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901141B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-fefa76d2e30245e1bf7f3a4eed5d4b44
출처 메모uspto-grants-2014_12