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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239811Generated: October 31, 2026

Acetonitrile → Belinostat acid

https://huagongshe.com/reaction/239811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium FluorideHCID 522689—
ReactantBelinostat acidHCID 22492441—
ProductBelinostat acidHCID 22492441—
ProductHCID 53487508HCID 53487508—

Reaction Conditions

Temperature80 °C

Reaction Steps

To the 30 gallon (˜136 L) reactor was charged the (E)-3-(3-phenylsulfamoyl-phenyl)-acrylic acid ethyl ester (5) (4.48 kg; 331.39 g/mol; 13.5 mol) along with 2 M aqueous sodium hydroxide (17.76 L; ˜35 mol). The mixture was heated to 40-50° C. and held at this temperature for 2 hours before sampling, at which point the reaction was deemed to be complete with no compound (5) being detected by HPLC. The batch was adjusted to pH 2.2 using 1 M aqueous hydrochloric acid while maintaining the batch temperature between 40-50° C. The product had precipitated and the batch was cooled to 20-30° C. and held at this temperature for 1 hour before filtering and washing the cake with water (8.9 L). The filtrate was discarded. The batch was allowed to condition on the filter overnight before being charged back into the reactor and slurried in water (44.4 L) at 40-50° C. for 2 hours. The batch was cooled to 15-20° C., held for 1 hour, and then filtered and the residue washed with water (8.9 L). The filtrate was discarded. The crude title compound (6) was transferred to an oven for drying at 45-55° C. under vacuum with a slight nitrogen bleed for 5 days (this was done for convenience) to give a white solid (3.93 kg, 97% yield). The moisture content of the crude material was measured using Karl Fischer (KF) titration and found to be <0.1% (w/w). To the 30 gallon (˜136 L) reactor was charged the crude compound (6) along with acetonitrile (47.2 L). The batch was heated to reflux (about 80° C.) and held at reflux for 2 hours before cooling to 0-10° C. and holding at this temperature overnight in order to precipitate the product. The batch was filtered and the residue was washed with cold acetonitrile (7.9 L). The filtrate was discarded and the residue was dried under vacuum at 45-55° C. for 21.5 hours. The title compound (6) was obtained as a fluffy white solid (3.37 kg, 84% yield with respect to compound (5)) with a purity of 99.89% (AUC) by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642809B2
Source datasetuspto-grants-2014_02
ORD IDord-bec593759914456e94a3101ae609393f
Source noteuspto-grants-2014_02