HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297500Generated: October 30, 2026
Diisopropylethylamine → HCID 58914773, compound
https://huagongshe.com/reaction/1297500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-3-nitropyridin-2-ylamine | HCID 2724035 | — |
| Reactant | HCID 58914793 | HCID 58914793 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 58914773 | HCID 58914773 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250443B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-c68fbe8b061f44b2b95255fe4014bd86 |
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| Source note | uspto-grants-2007_07 |
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