HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055075Generated: October 29, 2026
2-Iodoxybenzoic acid → HCID 86714755, compound
https://huagongshe.com/reaction/1055075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | HCID 71247355 | HCID 71247355 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86714755 | HCID 86714755 | — |
Reaction Steps
To a solution of racemic 3-((5-fluoro-2-(5-fluoro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)-4,4-dimethylpentan-1-ol, 82a, (1.60 g, 3.10 mmol) in THF (64 mL) was added 2-iodoxybenzoic acid (Ibx) (3.86 g, 6.21 mmol). The reaction mixture was heated to reflux under at atmosphere of nitrogen for 30 minutes. After cooling the mixture to room temperature, the solids were filtered. An aqueous saturated NaHCO3 solution was added to the filtrate and the biphasic mixture was stirred for 30 minutes. The mixture was further diluted with dichloromethane and the phases separated. The aqueous layer was extracted again with dichloromethane. The combined organic phases were dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified via silica gel chromatography (EtOAc/Hexanes) to afford 1.59 g of the desired product
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09394302B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-021467688ef04dad8868c8a0493e6247 |
|---|
| Source note | uspto-grants-2016_07 |
|---|