HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114567Generated: October 30, 2026
N-Iodosuccinimide → HCID 178468251, compound
https://huagongshe.com/reaction/2114567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | (R)-1-[6-(2,4-Difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol | HCID 68879888 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178468251 | HCID 178468251 | 109.3% |
Reaction Steps
N-iodo succinimide (35 mg. 0.157 mmol) was dissolved in 3 mL of DMF, and (R)-1-[6-(2,4-Difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol (42 mg, 0.131 mmol) was added. The reaction mixture was heated to 80° C. for two hours, after which an additional 35 mg of N-iodo succinimide was added. After heating for two more hours at 80° C., an additional 35 mg of N-iodo succinimide was added. The reaction mixture was heated at 80° C. for 5 more hours, then was cooled to room temperature. The reaction mixture was quenched by addition to water, and was partitioned between water and ethyl acetate. The organic layer was separated, dried over MgSO4, filtered, and evaporated under reduced pressure to give 64 mg of 1-[6-(2,4-Difluoro-phenoxy)-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol. Mass Spec. M+H=448.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07435731B2 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-70bea1e428ec4654885bbf07f8e211ea |
|---|
| Source note | uspto-grants-2008_10 |
|---|