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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-iodo-5-nitro-1H-indole-1-carboxylateHCID 40428559—
ReactantHCID 86709776HCID 86709776—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 67959775HCID 6795977530.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090593B2
Source datasetuspto-grants-2015_07
ORD IDord-f556da950a244f36a015c6e3baa701cb
Source noteuspto-grants-2015_07