HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059574Generated: October 31, 2026
N-Iodosuccinimide → HCID 178478409, compound
https://huagongshe.com/reaction/2059574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178478409 | HCID 178478409 | — |
Reaction Steps
To a 250 ml round-bottomed flask, protected from light with aluminum foil, are added 4-chloro-7H-pyrrolo[2,3-d]pyrimidine 1 (2.15 g, 14.0 mmol) and N-iodosuccinimide (3.37 g, 14.98 mmol) dissolved in anhydrous DMF. The reaction mixture is stirred at room temperature under nitrogen for 16 hrs. The solvent is removed in vacuo, and the residue is dissolved in methylene chloride (250 ml). The reaction mixture is washed with brine (50 ml), and the organic layer is separated, dried over Na2SO4, and concentrated in vacuo. The crude residue is purified by flash-chromatography on silica gel and eluted with 60% EtOAc in cyclohexane. Fractions containing the desired product (TLC) are pooled and evaporated to afford 4-chloro-5-iodo-pyrrolo[2,3-d]pyrimidine as a pale-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278282B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-60b9a4d18aac4daf82bf67d2b6f5e56c |
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| Source note | uspto-grants-2012_10 |
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