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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433763Generated: October 29, 2026

RO5068760 → HCID 57935194, compound

https://huagongshe.com/reaction/1433763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRO5068760HCID 17757766—
SolventMethanolHCID 887—
ProductHCID 57935194HCID 5793519444%

Reaction Steps

(2S,3S)-2-{(R)-4-[4-((R)-2,3-Dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-N-(2-fluoro-4-iodo-phenyl)-3-phenyl-butyramide (prepared as described in example 56) (160 mg, 0.25 mmol) was dissolved in methanol (10 ml) and allowed to stir for 48 hours at ambient temperature followed by warming to 50° C. for an additional 6 hours. The solvent was removed in vacuo and the residue was then purified by super-critical fluid chromatography using a Chiracel OD column eluted with carbon dioxide at 100 bar and 30° C. containing 35% methanol in acetonitrile eluted at 2 mL/minute. The second eluted compound was collected and concentrated in vacuo to obtain (2S,3S)-2-{(S)-4-[4-((R)-2,3-dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-N-(2-fluoro-4-iodo-phenyl)-3-phenyl-butyramide as a colorless solid (35 mg, 44%). The compound eluted first was identical with (2S,3S)-2-{(R)-4-[4-((R)-2,3-dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-N-(2-fluoro-4-iodo-phenyl)-3-phenyl-butyramide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612212B2
Source datasetuspto-grants-2009_11
ORD IDord-79ebbf3a4a514f0fa31ae5d13b9c67bc
Source noteuspto-grants-2009_11