HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957114Generated: November 2, 2026
2-Butanamine, 2-methyl- → 6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxaline
https://huagongshe.com/reaction/1957114
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Butanamine, 2-methyl- | HCID 68986 | — |
| Reactant | 5-[(2-Chloroethyl)pyrazol-1-ylmethyl]-6,7-dichloro-2,3-dimethoxyquinoxaline | HCID 54339196 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxaline | HCID 23224988 | 38% |
Reaction Steps
A mixture of 5-[(2-chloroethyl)pyrazol-1-ylmethyl]-6,7-dichloro-2,3-dimethoxyquinoxaline (150 mg, 0.37 mmol), 1,1-dimethyl-1-propylamine (3 mL) and ethanol (5 mL) were heated in a closed vessel at 105° C. for 7 hours. The mixture was cooled, the solvent was removed under reduced pressure, and the residue was dissolved in ethyl acetate (75 mL). The solution was washed with saturated aqueous sodium bicarbonate, dried (MgSO4) and concentrated under reduced pressure. Purification by flash chromatography (elution with dichloromethane, then an ethyl acetate/methanol/triethylamine gradient) gave 6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxaline (65 mg, 38%), as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05783572 |
|---|
| Source dataset | uspto-grants-1998_07 |
|---|
| ORD ID | ord-7e8695b6787e4c51a6b28f32700ac456 |
|---|
| Source note | uspto-grants-1998_07 |
|---|