HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068804Generated: October 30, 2026
2-(4-Aminophenyl)ethylamine → HCID 21190172, compound
https://huagongshe.com/reaction/1068804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(4-Aminophenyl)ethylamine | HCID 72895 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 15472383 | HCID 15472383 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21190172 | HCID 21190172 | 33.6% |
Reaction Steps
To a solution of 1.63 g (12.0 mmol) of 2-[4-(amino)phenyl]ethylamine and 1.68 g (13 mmol) of N,N-diisopropylethylamine in 40 ml of acetonitrile was added a solution of 3.50 g (10.0 mmol) of 5-ethoxycarbonyl-3-trichloroacetylimidazo[1,2-a]pyridine in 10 ml of acetonitrile. The mixture was stirred for one hour at room temperature. The resulting crystalline precipitates were collected by filtration, washed with acetonitrile and dried to afford 1.03 g of the desired compound (33.6%, a yellow crystals). The filtrate was concentrated. The residne was crystallized from acetonitrile-methylene chloride. Crystalline precipitatse were collected by filtration, washed with acetonitrile to afford 1.60 g of the desired compound (52.1%, a yellow crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251905B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-1ce0dc9bb6c34fcb8aee204f94cab4a5 |
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| Source note | uspto-grants-2001_06 |
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