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HRID 508631作成日:2026年10月25日

Dichloromethane → Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamate

https://huagongshe.com/reaction/508631

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium BicarbonateHCID 516892—
反応物2,2-Difluoro-1,3-benzodioxole-5-carbonyl chlorideHCID 2774064—
反応物Tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamateHCID 57993236—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamateHCID 57993507—

反応条件

温度-20 °C

反応手順

A solution of tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamate (50 mg, 0.19 mmol) and TEA (135 μL, 0.972 mmol) in a mixture of 1:1 CH2Cl2:THF (2.5 mL) was treated with 2,2-difluorobenzo[d][1,3]dioxole-5-carbonyl chloride (51 mg, 0.23 mmol). The resulting solution was stirred overnight, then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigorously and allowed to separate for 15 minutes. After separation, the mixture was cooled to −20° C. until the aqueous layer was frozen. The organic layer was then poured off and the solvent was removed under reduced pressure at 50° C. The resulting residue was purified by HiTOPs.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096522B2
出典データセットuspto-grants-2015_08
ORD IDord-d3b621205b19478fa6934853a6adb824
出典メモuspto-grants-2015_08