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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781916Generated: October 26, 2026

Hydrochloric Acid → 5-(2-Anilino-4-thiazolyl)-2,3-dihydroxybenzonitrile hydrochloride

https://huagongshe.com/reaction/1781916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenylthioureaHCID 676454—
Reactant5-(Bromoacetyl)-2,3-dihydroxybenzonitrileHCID 21459065—
SolventDimethylformamideHCID 6228—
Product5-(2-Anilino-4-thiazolyl)-2,3-dihydroxybenzonitrile hydrochlorideHCID 21459182—

Reaction Steps

3.8 g of 5-(bromoacetyl)-2,3-dihydroxybenzonitrile dissolved in 25 ml of N,N-dimethylformamide are treated with N-phenylthiourea and stirred at 100° for 5 hours. Thereafter, the solvent is removed by evaporation. The residue is treated with 200 ml of 1N sodium carbonate solution and extracted three times with 100 ml of methylene chloride each time. The combined organic phases are washed with water, dried over sodium sulfate and evaporated. The residue is chromatographed on 30 g of silica gel with ethyl acetate. The thus-obtained crude product is treated with 40 ml of 1N hydrochloric acid, evaporated and crystallized from acetone. There is obtained 5-(2-anilino-4-thiazolyl)-2,3-dihydroxybenzo- nitrile hydrochloride of m.p. 245°-247°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-21b99671dadd41de8b36e62c0a1d232f
Source noteuspto-grants-1997_05