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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260322Generated: October 27, 2026

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

https://huagongshe.com/reaction/2260322

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 numberUS05476875
Source datasetuspto-grants-1995_12
ORD IDord-1f7603515c364209b46d94db8f7ec189
Source noteuspto-grants-1995_12