HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783387Generated: October 30, 2026
2-(Tributylstannyl)pyrazine → HCID 57590475, compound
https://huagongshe.com/reaction/1783387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Tributylstannyl)pyrazine | HCID 2737316 | — |
| Reactant | HCID 57590468 | HCID 57590468 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57590475 | HCID 57590475 | 7% |
Reaction Steps
A solution of 3-[4-[2-(7-bromo-4-methoxy-6-azaindol-3-yl)-2-oxoacetyl]piperazin-1-yl]-4-phenyl-cyclobut-3-ene-1,2-dione (0.030 g, 0.057 mmol) and 2-tributylstannylpyrazine (0.025 g, 0.069 mmol) in dioxane (3 mL) was purged with Ar and then Pd(PPh3)4 (0.020 g, 0.017 mmol) was added, the reactor was sealed and the mixture was heated at 90° C. for 16 h. The cooled reaction mixture was diluted with EtOAc, washed (1M aqueous KF, brine), dried (Na2SO4) and evaporated to give a solid. Purification of this material by preparative HPLC (C-18/10-90% MeCN-5 mmolar aqueous NH4OAc) gave the title compound (0.002 g, 7%) as a yellow solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07501419B2 |
|---|
| Source dataset | uspto-grants-2009_03 |
|---|
| ORD ID | ord-0a802b3ca9524f2a8f42c6e306d1dcbd |
|---|
| Source note | uspto-grants-2009_03 |
|---|