HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529296Generated: November 1, 2026
2-Chloro-6-(tributylstannyl)pyrazine → HCID 86709767, compound
https://huagongshe.com/reaction/1529296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-6-(tributylstannyl)pyrazine | HCID 11774057 | — |
| Reactant | tert-butyl 5-(2,6-difluorophenyl)-3-iodo-1H-indole-1-carboxylate | HCID 67958266 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86709767 | HCID 86709767 | 35.1% |
Reaction Steps
A glass microwave reaction vessel was charged with 2-chloro-6-(tributylstannyl)pyrazine (177 mg, 0.439 mmol) and tert-butyl 5-(2,6-difluorophenyl)-3-iodo-1H-indole-1-carboxylate (200 mg, 0.439 mmol) in DMF (2.5 mL) followed by CuI (18 mg, 0.044 mmol) and Pd(PPh3)4 (50.8 mg, 0.044 mmol). The reaction mixture was stirred and heated in a Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Uppsala, Sweden) at 100° C. for 40 min, and then the mixture was diluted with DCM. The organic layer was separated, washed with water (20 mL×4), dried over Na2SO4, filtered and concentrated. The residue was purified with silica gel chromatography (eluting with 0-5% EtOAc in Hexanes) to give tert-butyl 3-(6-chloropyrazin-2-yl)-5-(2,6-difluorophenyl)-1H-indole-1-carboxylate (68.0 mg, 0.154 mmol, 35.0% yield) as a white solid. MS (ESI, pos. ion) m/z: 442 (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-0614f5687eb045a490754aa523f07600 |
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| Source note | uspto-grants-2015_07 |
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