HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529355Generated: November 1, 2026
tert-Butyl 3-iodo-5-nitro-1H-indole-1-carboxylate → HCID 67959775, compound
https://huagongshe.com/reaction/1529355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 3-iodo-5-nitro-1H-indole-1-carboxylate | HCID 40428559 | — |
| Reactant | HCID 86709776 | HCID 86709776 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67959775 | HCID 67959775 | 30.2% |
Reaction Steps
To a mixture of 3-Iodo-5-nitro-indole-1-carboxylic acid tert-butyl ester (480 mg, 1.23 mmol) and tert-butyl 1-(6-(tributylstannyl)pyrazin-2-yl)piperidin-4-ylcarbamate 1d (700 mg, 1.23 mmol) in DMF (4.8 mL) was purged with argon gas for 5 min and added Cut (352 mg, 1.84 mmol) and palladium tetrakis (171 mg, 0.15 mmol). The resulting mixture was purged with argon gas for 5 min and stiffed under nitrogen atmosphere at 90° C. 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. Purification was carried out by column chromatography to obtain the title compound as a white solid (200 mg, 30%). MS (ESI, pos. ion) m/z: 539.3 (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-f556da950a244f36a015c6e3baa701cb |
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| Source note | uspto-grants-2015_07 |
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