Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180401Generated: October 30, 2026

Hydrochloric Acid → HCID 85064118, compound

https://huagongshe.com/reaction/2180401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 73989424HCID 73989424—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 85064118HCID 85064118—

Reaction Steps

To a suspension of hydroxylamine hydrochloride (0.31 g, 4.40 mmol) in tetrahydrofuran (5 ml) a saturated NaHCO3 solution (6.8 ml) was added and the resultant mixture was stirred at ambient temperature for 10 min. To the reaction mixture a solution of crude 3-{3-[(pyridin-3-ylmethyl)-sulfamoyl]-phenyl}-acryloyl chloride (16b) (0.29 g, 0.86 mmol) in tetrahydrofuran (5 ml) was added and the mixture was stirred at ambient temperature for one hour. The reaction mixture was poured into water, the obtained solution was acidified with 2N HCl to pH˜5 of the reaction medium and extracted with ethyl acetate. The organic layer was washed successively with water and saturated NaCl, then the solvent was removed. The residue was washed with hot ethyl acetate and methanol affording the title compound (0.12 g, 37%). M.p. 191° C. 1H NMR (DMSO-d6, HMDSO) δ: 4.05 (2H, d, J=6.4 Hz); 6.56 (1H, d, J=16.0 Hz); 7.16-8.05 (7H, m); 8.16-8.49 (3H, m); 9.12 (1H, br s); 10.80 (1H, br s). HPLC analysis on Symmetry C18 column: impurities 8% (column size 3.9×150 mm; mobile phase acetonitrile—0.1M phosphate buffer (pH 2.5), 10:90; sample concentration 0.4 mg/ml; flow rate 1.3 ml/min; detector UV 270 nm). Anal. Calcd for C15H15N3O4S containing 0.5% of inorganic impurities, %: C, 53.77; H, 4.51; N, 12.54. Found, %: C, 53.72; H, 4.33; N, 12.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888027B2
Source datasetuspto-grants-2005_05
ORD IDord-b10a25c8bf1b490fa276d2c6add99adf
Source noteuspto-grants-2005_05