戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1962861作成日:2026年10月27日

Triacetoxyperiodinane → (3-Ethynyl-quinolin-6-yloxy)-N-(1-methoxymethyl-1-methyl-2-oxo-ethyl)-2-methylsulfanyl-acetamide

https://huagongshe.com/reaction/1962861

反応式

関与物質

役割名称HCID仕込み量
反応物TriacetoxyperiodinaneHCID 159087—
反応物Sodium BicarbonateHCID 516892—
反応物2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamideHCID 59565371—
溶媒DichloromethaneHCID 6344—
生成物(3-Ethynyl-quinolin-6-yloxy)-N-(1-methoxymethyl-1-methyl-2-oxo-ethyl)-2-methylsulfanyl-acetamideHCID 5956527860.3%

反応手順

A solution of 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide (200 mg) in dry CH2Cl2 (15 ml) was treated with Dess-Martin periodinane (295 mg). The mixture was stirred at room temperature during 1 h then poured on sat aq NaHCO3. After separation the water phase was washed twice with CH2Cl2 The combined organic phases were washed with brine, dried over sodium sulfate, filtered and evaporated. The crude residue was purified by column chromatography (cyclohexane/ethyl acetate 1:1) to give (3-Ethynyl-quinolin-6-yloxy)-N-(1-methoxymethyl-1-methyl-2-oxo-ethyl)-2-methylsulfanyl-acetamide (120 mg) as yellowish oil 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-d725e15165c049f390a39b5233ffff83
出典メモuspto-grants-2013_04