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 | 74.6% |
Reaction Steps
4-Chloro-7H-pyrrolo[2,3-d]pyrimidine 10.75 g (70 mmol) and N-iodosuccinimide (16.8 g, 75 mmol) were dissolved in 400 ml of dry DMF and left at ambient temperature in the darkness over night. The solvent was evaporated. The yellow residue was suspended in hot 10% solution of Na2SO3, filtered, washed twice with hot water and crystallized from ethanol to yield 14.6 g (74.6%) of the title compound as off-white crystals. The mother liquid was evaporated up to ⅓ volume and crystallized again from ethanol to give 2.47 g (12.3%) of the title product. The total yield is close to 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144868B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-6dee9b080f4e4c96abb9c9f80434e8b8 |
| Source note | uspto-grants-2006_12 |