Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604371Generated: November 1, 2026

Isobutanol → Methyl 2-[N-(5-bromo-2-(2-methylpropoxy)benzyl)-N-ethylamino]pyridine-5-carboxylate

https://huagongshe.com/reaction/1604371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutanolHCID 6560—
ReactantTriphenylphosphineHCID 11776—
Reactantmethyl 2-[N-(5-bromo-2-propoxybenzyl)-N-ethylamino]pyridine-5-carboxylateHCID 22622503—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-[N-(5-bromo-2-(2-methylpropoxy)benzyl)-N-ethylamino]pyridine-5-carboxylateHCID 2262249160.6%

Reaction Steps

A solution of the methyl-2-[N-(5-bromo-2-(hydroxy-benzyl)-N-ethylamino]pyridine-5-carboxylate (reference example 1, paragraph 7) (0.5 g, 1.37 mmol) in THF (15 ml) was treated with triphenylphosphine (0.39 g, 1.49 mmol) and diazoethyldicarboxylate. The reaction was stirred at ambient temperature for five minutes and then isobutyl alcohol (0.152, 2.06 mmol,) added. The reaction was then stirred at ambient temperature for 18 hours. partitioned between ethyl acetate and water and the aqueous layer washed with ethyl acetate (×2). The organic layers were combined, washed with water and brine, dried (MgSO4) and evaporated. The residue was subjected to chromatography (eluant: ethyl acetate/hexane) to give the title compound (0.35 g, 60%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994353
Source datasetuspto-grants-1999_11
ORD IDord-967b209678054b8f9f725e5a74c6c7a3
Source noteuspto-grants-1999_11