Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455991Generated: November 3, 2026

Sodium hydride → HCID 22105557, compound

https://huagongshe.com/reaction/1455991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(Benzyloxy)-4-bromo-2-(bromomethyl)benzeneHCID 11783220—
ReactantHCID 22105664HCID 22105664—
SolventDimethylformamideHCID 6228—
ProductHCID 22105557HCID 2210555773.7%

Reaction Steps

To a solution of ethyl 5-(tert-butoxycarbonylamino)pyrazine-2-carboxylate (10.7 g 0.04 mol) in DMF (160 ml) at 20° C., under argon atmosphere, was added sodium hydride dispersion (50% in oil, 1.85 g, 0.04 mol) and stirred for 1 hour until effervescence ceased. Next was added 2-benzyloxy-5-bromobenzylbromide (14.3 g, 0.04 mol) and stirring continued at 20° C. under argon for 2 hours. The solvent was evaporated at reduced pressure and the residue partitioned between dichloromethane (500 ml) and water (250 ml), the organic layer was dried over magnesium sulphate and evaporated at reduced pressure to give a crude solid (21 g). Purification was by chromatography on silica, eluting with 5% ethyl acetate in dichloromethane to give ethyl 5-(N-(2-benzyloxy-5-bromobenzyl)-N-tert-butoxycarbonylamino)pyrazine-2-carboxylate as a white solid (16 g, mp 116°-7° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843942
Source datasetuspto-grants-1998_12
ORD IDord-e1c98a2718534a76830c6d35bb456d7d
Source noteuspto-grants-1998_12