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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11476생성일: 2026년 10월 25일

Hexane → cis-1-[2-(1-Adamantyl)ethyl]-1-pentyl-3-[2-(4-pyridyl)cyclopropylmethyl]urea

https://huagongshe.com/reaction/11476

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물ChloroiodomethaneHCID 11644—
반응물Ammonium ChlorideHCID 25517—
반응물(Z)-1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)-2-propenyl]ureaHCID 10294976—
반응물HCID 178418750HCID 178418750—
용매1,2-DichloroethaneHCID 11—
용매Ethyl AcetateHCID 8857—
생성물cis-1-[2-(1-Adamantyl)ethyl]-1-pentyl-3-[2-(4-pyridyl)cyclopropylmethyl]ureaHCID 671187303.5%

반응 단계

A 1.0 M solution of diethylzinc in hexane (3.1 ml, 3.1 mmol) and chloroiodomethane (0.44 ml, 6.1 mol) were added to a solution of (Z)-1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)-2-propenyl]urea (Compound No. 1-111) in anhydrous 1,2-dichloroethane (3 ml) under a nitrogen atmosphere and ice-cooling, and the mixture was stirred for one hour. A saturated aqueous ammonium chloride solution (10 ml) was added to the reaction mixture under ice-cooling, and the whole was stirred at room temperature for 20 minutes and distributed with ethyl acetate (20 ml) and a saturated aqueous ammonium chloride solution (10 ml). The organic layer was washed with a saturated aqueous sodium chloride solution (10 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give 9.0 mg (3.5%) 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-b777ff91edf849818303f364dcaebf2f
출처 메모uspto-grants-2006_08