Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062645Generated: October 26, 2026

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

https://huagongshe.com/reaction/1062645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropyl EtherHCID 7914—
Reactanttert-butyl N-(4-methylpyridin-2-yl)carbamateHCID 11063648—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
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 1.6 M n-butyllithium/hexane solution (140 mL, 0.23 mol) was added dropwise with stirring. After completion of the dropwise addition, the mixture was stirred at room temperature for 30 min and cooled to −78° C. A solution of N-(4-methoxybenzoyl)propyleneimine (25 g, 0.13 mol) in anhydrous tetrahydrofuran (50 mL) was added dropwise. After completion of the dropwise addition, the mixture was stirred at room temperature for 2 h. To the reaction mixture were added water (100 mL) and isopropyl ether (300 mL), and the obtained crude crystals were collected by filtration. The crude crystals were recrystallized from tetrahydrofuran-hexane to give the title compound (23 g, yield 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962933B1
Source datasetuspto-grants-2005_11
ORD IDord-2e1c2879308049c4b0676845538ff3f4
Source noteuspto-grants-2005_11