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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-[2-(1-Adamantyl)ethyl]-3-[3-(t-butyldimethylsilyloxy)-3-(4-pyridyl)propyl]-1-pentylurea | HCID 21974159 | — |
| 용매 | Hydrochloride methanol | HCID 21893726 | — |
| 생성물 | 1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylurea | HCID 21973986 | 55.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07923461B2 |
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| 출처 데이터셋 | uspto-grants-2011_04 |
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| ORD ID | ord-553f51229e454e10b20c1f40e88baed0 |
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| 출처 메모 | uspto-grants-2011_04 |
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