HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045721Generated: October 30, 2026
Cesium carbonate → 8-Methoxy-5-(thiophen-2-yl)-[1,2,4]triazolo[4,3-a]pyrazine
https://huagongshe.com/reaction/1045721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 5-Bromo-8-methoxy-[1,2,4]triazolo[4,3-A]pyrazine | HCID 58446980 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Methoxy-5-(thiophen-2-yl)-[1,2,4]triazolo[4,3-a]pyrazine | HCID 58447037 | 99% |
Reaction Steps
A 50 mL round bottom flask was charged with 5-bromo-8-methoxy-[1,2,4]triazolo[4,3-a]pyrazine (0.25 g, 1.1 mmol), thiophen-2-ylboronic acid (280 mg, 2.2 mmol), Pd(PPh3)4 (190 mg, 0.16 mmol), Cs2CO3 (530 mg, 1.6 mmol), 1,4-dioxane (11 mL) and water (4 mL). The resulting mixture was heated under N2 at 100° C. overnight. Work-up: the reaction mixture was filtered. The filter cake was washed with EtOAc (10 mL) and the filtrate was extracted with more EtOAc (10 mL×3). The combined organic solutions were washed with brine, dried over anhydrous Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:50 methanol/dichloromethane, to afford 0.25 g (99%) of the product as a yellow solid. MS m/z: 233 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569300B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-253db3cef78643d1bb071e927acd7f4c |
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| Source note | uspto-grants-2013_10 |
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