HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 6-Chloro-7-iodo-7-deazapurine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-7-iodo-7-deazapurine | HCID 14809281 | 72% |
Reaction Steps
A mixture of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (3.0 g, 20 mmol) and NIS (4.9 g, 20.1 mmol) in DMF (100 mL) was stirred in darkness at room temperature overnight. Then the mixture was concentrated in vacuo. The residue was treated with 10% Na2SO3 and filtered to give 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine (4.0 g, yield 72%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-73d6df0133f8487b9ca3c8eb415e2d25 |
| Source note | uspto-grants-2014_02 |