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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892055생성일: 2026년 10월 26일

Ammonium Chloride → 2-(3-ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-cyclobutyl)-2-methylsulfanyl-acetamide

https://huagongshe.com/reaction/1892055

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물(1-Aminocyclobutyl)methanolHCID 21624254—
반응물(3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acidHCID 59565474—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물2-(3-ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-cyclobutyl)-2-methylsulfanyl-acetamideHCID 59565328331.1%

반응 단계

To a solution of (3-ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acid (1.10 g) in CH3CN (40 ml) was added Et3N (2.25 ml), AHOBT (0.06 g), TBTU (1.50 g) and (1-amino-cyclobutyl)-methanol (0.06 g) at room temperature, under nitrogen atmosphere. The mixture was stirred at the same temperature during 1 hour, then poured into sat aq NH4Cl and extracted with ethyl acetate (2×20 ml). The organic phase was separated and washed with aq Na2S2O3 and sat. aq. NaCl then dried over anhydrous sodium sulphate, filtered and evaporated under vacuum. Purification by flash chromatography (ethyl acetate/cyclohexane, 2/1) gave 2-(3-ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-cyclobutyl)-2-methylsulfanyl-acetamide (0.70 g) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507509B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-d63b4808df2e48fd8b1f5b4f5eca3baf
출처 메모uspto-grants-2013_08