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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212331Generated: October 29, 2026

Diisopropyl Ether → 1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanone

https://huagongshe.com/reaction/2212331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
Reactanttert-butyl N-(4-methylpyridin-2-yl)carbamateHCID 11063648—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
Product1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanoneHCID 1161709269%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-tert-butoxycarbonylamino-4-methylpyridine (20 g, 97 mmol) in anhydrous tetrahydrofuran (300 mL) was cooled to −78° C. and a solution of 1.6 M n-butyllithium in hexane (140 mL, 0.22 mol) was added dropwise with stirring. After complete addition, the mixture was stirred at room temperature for 30 minutes. And then, the mixture was cooled to −78° C. A solution of N-(4-methoxybenzoyl)propyleneimine in anhydrous tetrahydrofuran (50 mL) was added dropwise to the mixture. After complete addition, the mixture was stirred at room temperature for 2 hours. Water (100 mL) and diisopropyl ether (300 mL) were added to the reaction mixture and the resulting crude crystals were collected by filtration. The crude crystals were recrystallized from tetrahydrofuran-hexane to obtain 23 g of the title compound (67 mmol, yield 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101899B1
Source datasetuspto-grants-2006_09
ORD IDord-e5eb43a7438c498ca0dee19ee4809187
Source noteuspto-grants-2006_09