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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931552Generated: November 3, 2026

Acetic Acid → HCID 68658794, compound

https://huagongshe.com/reaction/1931552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 59312674HCID 59312674—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 68658794HCID 6865879477.8%

Reaction Steps

Palladium hydroxide on carbon (10.6 mg, 0.015 mmol) and acetic acid (17 μl, 0.297 mmol) were added to a stirred solution of (1S,4aR,6aS,7R,8R,10aR,10bR,12aR,14R,15R)-15-[[(2R)-2-amino-2,3,3-trimethylbutyl]oxy]-14-[5-(4-cyanophenyl)-1H-1,2,4-triazol-1-yl]-8-[(1R)-1,2-dimethylpropyl]-1,6,6a,7,8,9,10,10a,10b,11,12,12a-dodecahydro-1,6a,8,10a-tetramethyl-4H-1,4a-propano-2H-phenanthro[1,2-c]pyran-7-carboxylic acid (Example 168, 52.5 mg, 0.060 mmol) in methanol (3.0 ml). The reaction mixture was degassed (3×) and purged with hydrogen before being placed under a hydrogen balloon. After 6 hours, the hydrogen balloon was removed. The reaction mixture was degassed (2×), diluted with methanol, and filtered through a pad of Celite. The filtrate was evaporated under reduced pressure to give a colorless residue. The residue was dissolved in methanol and purified using a single HPLC run on a 30×150 mm Sunfire Prep C18 OBD 10 μm column by eluting with acetonitrile/water+0.1% TFA. The total flow rate was 20 ml/min and the HPLC method employed a 17 minute 20%-100% acetonitrile/water gradient followed by a 2 minute acetonitrile flush. The product fractions were combined, the solvent was evaporated under reduced pressure, and the residue was lyophilized from ethanol and benzene to give the title compound (35.4 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188085B2
Source datasetuspto-grants-2012_05
ORD IDord-4caca49537af41bd80f408515b451be1
Source noteuspto-grants-2012_05