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HRID 473953作成日:2026年10月26日

Diisopropyl diazene-1,2-dicarboxylate → Methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate

https://huagongshe.com/reaction/473953

反応式

関与物質

役割名称HCID仕込み量
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物Cyclopentanecarboxylic acid, 3-hydroxy-, methyl esterHCID 520596—
反応物HCID 178515818HCID 178515818—
溶媒TolueneHCID 1140—
生成物Methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylateHCID 5857790751%

反応手順

A solution of methyl 3-hydroxycyclopentanecarboxylate A-11 (500.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) was added to a solution of 5-bromopyridin-2-ol (522.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) at room temperature. Diisopropyl azodicarboxylate (1.57 g, 6.00 mmol) was then added dropwise, and the yellow-orange solution was stirred at room temperature for 12 h. The reaction mixture was then quenched with methanol (1.0 mL) and concentrated to dryness under reduced pressure. The residue was purified by flash column chromatography on silica gel (hexanes to ethyl acetate gradient) to give methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate A-12 (462.0 mg, Yield=51%). MS (ESI), [M+Na]+ 321, 323.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637507B2
出典データセットuspto-grants-2014_01
ORD IDord-9b2e0014adbe449db1634b351e2ff97b
出典メモuspto-grants-2014_01