HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272961Generated: November 1, 2026
Sodium Bicarbonate → HCID 71765497, compound
https://huagongshe.com/reaction/2272961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | HCID 2773987 | — |
| Reactant | HCID 71765496 | HCID 71765496 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71765497 | HCID 71765497 | — |
Reaction Steps
Under nitrogen, a suspension of 141 mg (0.486 mmol) 3-(4-bromo-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one, 111 mg (0.534 mmol) 1-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole and 49 mg (0.58 mmol) sodium hydrogen carbonate in 1 ml DMF and 0.5 ml water is heated to 40° C. Then 6.8 mg (0.010 mmol) bis(triphenylphosphine)-palladium(II)-chloride is added. The reaction mixture is heated to 80° C. and stirred at this temperature for 20 hours. The reaction mixture is cooled to room temperature and excess water is added. The resulting precipitate is filtered off and washed with water. The residue is chromatographed on a silica gel column with methanol/dichloromethane as eluent to give 3-[4-(1-methyl-1H-pyrazol-4-yl)phenyl]-2H-pyrrolo[1,2-a]pyrazin-1-one as light yellow crystals; HPLC/MS 2.09 min (B), [M+H] 291;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120805B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8d973d385e4644fa9eb6b3d4e9c99077 |
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| Source note | uspto-grants-2015_09 |
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