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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274557Generated: October 25, 2026

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

https://huagongshe.com/reaction/274557

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 numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-9865c62f45bf4d08857121dbab89b3a6
Source noteuspto-grants-1995_02