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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670176Generated: October 30, 2026

Hydrochloric Acid → N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-phenylethynyl-benzamide

https://huagongshe.com/reaction/1670176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Hydroxy-2-(4-phenylethynyl-benzoylamino)-butyric acid methyl esterHCID 66677268—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-phenylethynyl-benzamideHCID 7559989855%

Reaction Steps

A solution of tolanoic-Thr methyl ester (4) (2.34 g, 7.0 mmol) in MeOH (20 ml) and DCM (30 ml) was added to a cooled (−10° C. bath) suspension of hydroxylamine HCl salt (4.81 g, 70.0 mmol) and NaOMe (4.16 g, 77.0 mmol) in MeOH (30 ml). Follow reaction by LCMS. After stirring for 2 hours, the reaction seems to stall at 50% completion. Add an additional 1 equivalent of NaOMe (0.416 g). After 3 hours, the reaction was 75% complete. Add an additional 0.5 equivalent of NaOMe (0.21 g). After 4 hours, the reaction was 90% complete. Add an additional 0.15 equivalent of NaOMe (0.064 g) for a total of 12.65 equivalents of NaOMe. The pH of the reaction was between 11-12 and had reacted about 95% completion. The reaction was diluted with EtOAc (500 ml) and washed with sat. aq. NaHCO3 (2×60 ml), 50% diluted brine (60 ml), sat. brine (60 ml), dried with Na2SO4, filtered and concentrated under reduced pressure. The residue was dissolved in minimal DMA. The product was purified by prep. HPLC using a reverse phase Ultro 120 C18 column running a 2% gradient (AcCN/water, 0.1% TFA). The purified fractions were lyophilized to dryness. The product as the TFA salt was dissolved in AcCN/water (50:50) (80 ml), 1N aq. HCl (13 equivalent) and lyophilized again to give 1.3 g of white powder in 55% yield and >97% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989660B2
Source datasetuspto-grants-2011_08
ORD IDord-2292b4a55d084c70958b75ed69603546
Source noteuspto-grants-2011_08