HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456121Generated: October 30, 2026
Triethylamine → 6-bromo-N2-(quinolin-6-ylmethyl)pyrazine-2,3-diamine
https://huagongshe.com/reaction/456121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Reactant | 6-(Aminomethyl)quinoline | HCID 1514384 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-bromo-N2-(quinolin-6-ylmethyl)pyrazine-2,3-diamine | HCID 45789418 | 92.2% |
Reaction Steps
A mixture of quinolin-6-ylmethanamine (3.6 g, 22.76 mmol), 3,5-dibromopyrazin-2-amine (5.75 g, 22.76 mmol) and triethyl amine (4.61 g, 45.5 mmol) was heated in a microwave to 130° C. for 5 h. The reaction mixture was diluted with CH2Cl2 and water and the organic layer was separated, washed with aqueous NH4Cl, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography with EA:Hexanes to provide 6-bromo-N2-(quinolin-6-ylmethyl)pyrazine-2,3-diamine (6.93 g, 92%). LCMS (method A): [MH]+=330, tR=4.89 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497368B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e40dc7c892c34dc88e6b34ebb557bcd2 |
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| Source note | uspto-grants-2013_07 |
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