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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11488생성일: 2026년 10월 23일

Sodium Sulfite → 1-[2-(1-Adamantyl)ethyl]-3-[3-oxo-3-(4-pyridyl)propyl]-1-pentylurea

https://huagongshe.com/ko/reaction/11488

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfiteHCID 24437—
반응물TriacetoxyperiodinaneHCID 159087—
반응물Sodium BicarbonateHCID 516892—
반응물1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylureaHCID 21973986—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물1-[2-(1-Adamantyl)ethyl]-3-[3-oxo-3-(4-pyridyl)propyl]-1-pentylureaHCID 2197411187.8%

반응 단계

1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (221 mg, 0.526 mmol) was added to a solution of 1-[2-(1-adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylurea (100 mg, 0.234 mmol) in anhydrous dichloromethane (2 ml) under ice-cooling, the temperature was raised to room temperature, and the mixture was stirred for one hour. The reaction mixture was cooled with ice again, ethyl acetate (10 ml), a saturated aqueous sodium sulfite solution (5 ml) and a saturated aqueous sodium hydrogencarbonate solution (5 ml) were added to the reaction mixture, and the whole was stirred for 15 minutes. The reaction mixture was distributed with ethyl acetate (50 ml) and water (10 ml), and the organic layer was washed with a saturated aqueous sodium sulfite solution (5 ml), a saturated aqueous sodium hydrogencarbonate solution (5 ml) and a saturated aqueous sodium chloride solution (25 ml) successively. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give 87.3 mg (87.8%) of the titled compound as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098226B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-e566d59fdc5441c397562ebe5a903995
출처 메모uspto-grants-2006_08