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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852544Generated: October 29, 2026

Water → HCID 59718926, compound

https://huagongshe.com/reaction/1852544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant2-Iodoxybenzoic acidHCID 108794—
ReactantHCID 178520972HCID 178520972—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 59718926HCID 5971892671.2%

Reaction Steps

Iodoxybenzoic acid (830 mg, 2.96 mmol) was added to a solution of trans-[4-(4-benzo-triazol-1-yl-pyrimidin-2-ylamino)-cyclohexyl]-methanol (640 mg, 1.97 mmol) in DMSO (10 mL) and the resulting mixture was stirred at RT for 23 hours. An additional aliquot of o-iodoxy-benzoic acid (830 mg, 2.96 mmol) was then added. After a few hours, the reaction was stopped. Water was added and the resulting mixture was stirred for 20 minutes, the solid formed was filtered and the filtrate was extracted 3 times with EtOAc. The combined organic extracts were washed once with water, dried over Na2SO4 and filtered; the solvent was evaporated under reduced pressure. The white solid formed was washed several times with EtOAc and it was combined with the previous obtained solid to give 789 mg of crude residue. This crude material was purified via flash chromatography (heptane/EtOAc, with a gradient from 20% to 50% of EtOAc) to give 452 mg (70% yield) of 4-(4-benzotriazol-1-yl-pyrimidin-2-ylamino)-cyclo-hexanecarbaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962622B2
Source datasetuspto-grants-2015_02
ORD IDord-9c9e7bb40b18400ea1dcd50298493214
Source noteuspto-grants-2015_02