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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1962860생성일: 2026년 10월 26일

Ammonium Chloride → 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide

https://huagongshe.com/reaction/1962860

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물HOAtHCID 181649—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물2-Amino-3-methoxy-2-methylpropan-1-olHCID 13375415—
반응물(3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acidHCID 59565474—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamideHCID 5956537135.4%

반응 단계

(3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acid (413 mg), 1-hydroxy-7-azabenzotriazole (HOAT) (267 mg), O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) (630 mg), 2-amino-3-methoxy-2-methyl-propan-1-ol (180 mg) and triethylamine (0.75 ml) in dry CH3CN (20 ml) were stirred at ambient temperature overnight. The reaction mixture was diluted with ethyl acetate and poured on sat. aq. NH4Cl. The water phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated. The residue was purified by column chromatography (cyclohexane/ethyl acetate 1:1) to give as a yellowish oil 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide (200 mg) as a mixture of diastereoisomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415272B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-ac84d842a74f41018a2c4cb78c4fc1ed
출처 메모uspto-grants-2013_04