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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075910생성일: 2026년 10월 27일

1-[2-(1-Adamantyl)ethyl]-3-[3-(t-butyldimethylsilyloxy)-3-(4-pyridyl)propyl]-1-pentylurea → 1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylurea

https://huagongshe.com/reaction/2075910

반응식

참여 물질

역할이름HCID투입량
반응물1-[2-(1-Adamantyl)ethyl]-3-[3-(t-butyldimethylsilyloxy)-3-(4-pyridyl)propyl]-1-pentylureaHCID 21974159—
용매Hydrochloride methanolHCID 21893726—
생성물1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylureaHCID 2197398655.3%

반응 단계

A solution of 1-[2-(1-adamantyl)ethyl]-3-[3-(t-butyldimethylsilyloxy)-3-(4-pyridyl)propyl]-1-pentylurea (Compound No. 1-138) (136 mg, 0.250 mmol) in 10% hydrogen chloride-methanol (2.3 ml) was stirred at room temperature for three days. The solvent was evaporated under reduced pressure, the residue was distributed with ethyl acetate (50 ml), water (30 ml) and a 1 N aqueous sodium hydroxide solution (20 ml), and the organic layer was washed with a saturated aqueous sodium chloride solution (40 ml). The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the titled compound (59.2 mg, colorless noncrystalline powder, 55.3%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07923461B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-553f51229e454e10b20c1f40e88baed0
출처 메모uspto-grants-2011_04