HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529367Generated: October 31, 2026
HCID 67960127, compound → HCID 67959731, compound
https://huagongshe.com/reaction/1529367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67960127 | HCID 67960127 | — |
| Reactant | HCID 86709776 | HCID 86709776 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67959731 | HCID 67959731 | 31% |
Reaction Steps
A mixture of tert-butyl 5-carbamoyl-3-iodo-1H-indole-1-carboxylate (460 mg, 1.42 mmol) and tert-butyl 1-(6-(tributylstannyl)pyrazin-2-yl)piperidin-4-ylcarbamate (1d) (807 mg, 1.42 mmol) in DMF (4.6 mL) was purged with argon gas for 5 min, added Cut (405 mg, 2.13 mmol), palladium tetrakis (170 mg, 0.14 mmol) and again purged with argon gas for 5 min. The reaction mixture was stirred at 90° C. under nitrogen atmosphere for 1 h. The reaction mixture was then poured into water. The resulting precipitate was collected by filtration. The filtrate was extracted with diethyl ether. The organic layer was concentrated and combined with the above precipitate to give the crude product, which was purified by column chromatography to obtain the title compound as a brown solid (200 mg, 31%). MS (ESI, pos. ion) m/z: 537.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-ec8ec0b3b65a4e5fa39b544a08893d22 |
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| Source note | uspto-grants-2015_07 |
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