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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33980생성일: 2026년 10월 24일

Ammonium Chloride → Bromo-9-(2-hydroxy-4-phenyl-butyl)-2-pyridin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-one

https://huagongshe.com/ko/reaction/33980

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-(2-Phenylethyl)oxiraneHCID 135955—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물3-Bromo-2-pyridin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-oneHCID 136092380—
용매DimethylformamideHCID 6228—
생성물Bromo-9-(2-hydroxy-4-phenyl-butyl)-2-pyridin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-oneHCID 59796509—

반응 단계

A mixture of 3-Bromo-2-pyridin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-one (0.45 g, 1.46 mmol) and 2-Phenethyl-oxirane (0.65 g, 4.4 mmol) in DMF (20 mL) was treated LiHMDS (5 mL, 5 mml). The mixture was heated at 90 C for 1 h and was cooled to room temperature. Saturated NH4Cl (50 mL) was added and the mixture was extracted with CH2Cl2 (3×20 mL). The organic phase was washed with H2O (3×), dried (Na2SO4), and concentrated. The resulting brown oil was chromatographed on silica with 1-5% (2N NH3-MeOH)/CH2Cl2 to afford the product as a white solid. M+1 457.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429594B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-bbb7399147164b5c850f0512570b1803
출처 메모uspto-grants-2008_09