HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220605Generated: October 26, 2026
Potassium Carbonate → {4-[4-(5-Methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-acetonitrile hydrochloride
https://huagongshe.com/reaction/220605
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Cyanomethyl)benzeneboronic acid | HCID 2773342 | — |
| Reactant | 3'-chloro-4-(5-methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl | HCID 86641663 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | {4-[4-(5-Methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-acetonitrile hydrochloride | HCID 68595251 | 72% |
Reaction Steps
Stir together 3′-chloro-4-(5-methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (177 mg, 0.480 mmol), 4-(cyanomethyl)benzene boronic acid (93 mg, 0.576 mmol), potassium carbonate (159 mg, 1.15 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.003 g, 0.003 mmol) and water (1 mL), in N,N-dimethylacetamide (2 mL) at room temperature under nitrogen, then heat at 120° C. for 4 hr. Cool to room temperature, dilute with water (5 mL) and extract with DCM (3×20 mL). Pass the combined DCM extracts through an IST Phase Separator Frit®, concentrate and purify (silica gel chromatography, eluting with 0:100 to 5:95 methanol:DCM). Dry in a vacuum oven over night, then dissolve the yellow oil in acetonitrile. Add 2 M aq. HCl and water then lyophilize to give the title compound as a dark yellow powder (168 mg, 72%). MS (ES): m/z=450.2 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202873B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-372a272feb7240b9a941637224db9531 |
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| Source note | uspto-grants-2012_06 |
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