HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707524Generated: October 31, 2026
Sodium Thiosulfate → 6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridine-2-carbaldehyde
https://huagongshe.com/reaction/707524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridin-2-yl)methanol | HCID 118162492 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridine-2-carbaldehyde | HCID 118162455 | — |
Reaction Steps
To a mixed solution of the crude product (402 mg) of (6-(3-(4-ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridin-2-yl)methanol described in Production Example 7-1 and dichloromethane (10.0 mL) was added Dess-Martin periodinane (787 mg, 1.86 mmol) at room temperature. The resultant mixture was stirred at room temperature for 2 hours. A saturated aqueous sodium thiosulfate solution and a saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture, and the resultant solution was extracted with dichloromethane. An organic layer was dried over anhydrous magnesium sulfate and then filtrated. The solvent was evaporated under a reduced pressure to give a crude product (362 mg) of the title compound. The product was used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09174998B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-3e84755133444c8890539bfaa4c6f992 |
|---|
| Source note | uspto-grants-2015_11 |
|---|