HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245907Generated: October 30, 2026
5-Aminopentan-1-ol → HCID 21913098, compound
https://huagongshe.com/reaction/1245907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminopentan-1-ol | HCID 75634 | — |
| Reactant | 2,4-Dichloro-5,6-dimethyl-3-nitropyridine | HCID 12109123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21913098 | HCID 21913098 | 34.4% |
Reaction Steps
A solution of 5-amino-1-pentanol (28.03 g, 271.4 mmol) in N,N-dimethylformamide (200 mL) was added over a period of 45 minutes to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (60.01 g, 271.4 mmol) in N,N-dimethylformamide. The reaction was stirred overnight and then the N,N-dimethylformamide was removed by vacuum distillation. The residue was dissolved in ethyl acetate (500 mL), washed with water (4×75 mL), dried over magnesium sulfate and then concentrated under reduced pressure. The crude product was dissolved in hot ethyl acetate (400 mL). Hexane was added until a clear solution was obtained then the mixture was allowed to cool to ambient temperature. The resulting precipitate was isolated by filtration and washed with cold hexane to provide 26.87 g of 5-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]pentan-1-ol as a solid. An additional 4.41 g was isolated from the filtrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07125890B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-65f6484fbbdf4f8da6aab39dc33187b5 |
|---|
| Source note | uspto-grants-2006_10 |
|---|