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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242022Generated: November 2, 2026

Diisopropylethylamine → HCID 58914773, compound

https://huagongshe.com/reaction/2242022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
ReactantHCID 58914793HCID 58914793—
SolventDimethylacetamideHCID 31374—
ProductHCID 58914773HCID 5891477375%

Reaction Steps

N-[1-(3-aminopropyl)-4-(4-ethylphenyl)pyrrol-3-yl] (tert-butoxy)carboxamide (1 eq) and 6-chloro-3-nitro-2-pyridylamine (1.2 eq) were dissolved in DMA with stirring under argon at rt. Hünig's Base (1.5 eq) was added to the clear dark brown solution which was heated to 60° C. for 12 hours until completion was determined by LC/MS and TLC, eluting with EtOAc/Hexane (3:2, v/v) (Rf=0.3). EtOAc was added to the reaction mixture which was then washed with water, brine, dried (Na2SO4), filtered, and concentrated to dryness to give the crude brown product. The brown residue was purified by silica column chromatography eluting with EtOAc/Hexane (24:26, v/v). After collecting the purified fractions and concentrating, the product was isolated as a light yellow solid (75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671049B2
Source datasetuspto-grants-2010_03
ORD IDord-7558f034bd8a437da482f1a18ca21226
Source noteuspto-grants-2010_03