戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1962860作成日:2026年10月26日

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

https://huagongshe.com/reaction/1962860

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物HOAtHCID 181649—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物2-Amino-3-methoxy-2-methylpropan-1-olHCID 13375415—
反応物(3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acidHCID 59565474—
溶媒AcetonitrileHCID 6342—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamideHCID 5956537135.4%

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415272B2
出典データセットuspto-grants-2013_04
ORD IDord-ac84d842a74f41018a2c4cb78c4fc1ed
出典メモuspto-grants-2013_04