HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570603Generated: November 2, 2026
Sodium Carbonate → [8-(3-Aminomethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyrazin-2-yl]-(3,5-dimethoxy-phenyl)-amine
https://huagongshe.com/reaction/570603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-(Aminomethyl)phenyl)boronic acid | HCID 2773203 | — |
| Reactant | (8-Chloro-[1,2,4]triazolo[1,5-a]pyrazine-2-yl]-(3,5-dimethoxy-phenyl)-amine | HCID 86694342 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | [8-(3-Aminomethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyrazin-2-yl]-(3,5-dimethoxy-phenyl)-amine | HCID 66583836 | — |
Reaction Steps
To a solution of (8-chloro-[1,2,4]triazolo[1,5-a]pyrazine-2-yl]-(3,5-dimethoxy-phenyl)-amine (0.2 g, 0.65 mmol, 1 eq) in a mixture of dimethoxy ethane (3 ml) and water (1 ml), 3-aminomethylphenyl boronic acid (0.28 g, 1.31 mmol, 2 eq), sodium carbonate (0.14 g, 1.31 mmol, 2 eq)) and dichlorobis(triphenyl-phospine)palladium (II) (0.023 g, 0.03 mmol, 5%) are taken in a microwave vial and heated at 120° C. for 2 hours. The reaction mixture is concentrated and the residue is taken in dichloromethane (10 ml×1), washed with brine solution (10 ml×1), the organic layer is dried over anhydrous MgSO4 and concentrated. The crude product obtained is purified by silica gel column using (230-400) mesh to get the titled product as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023851B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b6dec6b7854a4deab300a40132862a9f |
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| Source note | uspto-grants-2015_05 |
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