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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29770Generated: October 30, 2026

Ethanol → 2-(6-Tert-butoxycarbonylamino-pyridin-3-ylmethyl)-3-butyl-2-ethoxycarbonyl-succinic acid diethyl ester

https://huagongshe.com/reaction/29770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium hydrideHCID 24758—
Reactant2-Butyl-3-ethoxycarbonyl-succinic acid diethyl esterHCID 13445020—
Reactanttert-Butyl (5-(bromomethyl)pyridin-2-yl)carbamateHCID 23030321—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(6-Tert-butoxycarbonylamino-pyridin-3-ylmethyl)-3-butyl-2-ethoxycarbonyl-succinic acid diethyl esterHCID 5424352578.6%

Reaction Steps

A solution of 2-butyl-3-ethoxycarbonyl-succinic acid diethyl ester (1 g, 3 mmol) and NaH (119 mg, 5 mmol) in DMF (20 ml) was stirred for 60 minutes at 0° C. under argon. (5-Bromomethyl-pyridin-2-yl)-carbamic acid tert-butyl ester (1.425 g, 5 mmol) was added and the mixture was stirred at room temperature for one week. Ethanol (1 ml) was added and the reaction was poured into H2O and extracted with ethyl acetate. The organic layer was washed with water and concentrated under reduced pressure. The product was purified by column chromatography (heptane/ethyl acetate, 4:1 to 1:1) to give 2-(6-tert-butoxycarbonylamino-pyridin-3-ylmethyl)-3-butyl-2-ethoxycarbonyl-succinic acid diethyl ester (1.2 g, 71.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423012B2
Source datasetuspto-grants-2008_09
ORD IDord-54ecf76dce5245d5a20e5eab56e19121
Source noteuspto-grants-2008_09