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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085359Generated: October 27, 2026

1-Amino-3-(3-carboxyphenyl)-2-thioxoimidazolidin-4-one → HCID 178426269, compound

https://huagongshe.com/reaction/2085359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Amino-3-(3-carboxyphenyl)-2-thioxoimidazolidin-4-oneHCID 22730986—
ReactantHCID 178426271HCID 178426271—
SolventEthanol, mixt. with methanolHCID 18681192—
ProductHCID 178426269HCID 17842626946%

Reaction Steps

Ethyl hydrazinoacetate hydrochloride (155 mg, 1.00 mmol) was added to a stirred solution of 3-isothiocyanatobenzoic acid (179 mg, 1.00 mmol) and di-isopropylethylamine (523 uL, 3.00 mmol) in dichloromethane (4 mL). The mixture was stirred for 96 h, evaporated under reduced pressure and partitioned between aqueous acetic acid and ethyl acetate. The organic extracts were washed with water, saturated aqueous sodium chloride, dried (magnesium sulfate) and evaporated under reduced pressure. The residue was chromatographed (silica gel, 5-15% methanol/ethyl acetate, then 20% methanol/ethyl acetate ±0.5% acetic acid) to give 1-amino-3-(3-carboxyphenyl)-2-thioxoimidazolidin-4-one (50 mg, 51%) contaminated with 6% uncyclised by-product, suitable for the next step. A solution of 1-amino-3-(3-carboxyphenyl)-2-thioxoimidazolidin-4-one (50 mg, 0.199 mmol) and 1-(3,4-dimethylphenyl)-5-hydroxy-3-methyl-1H-pyrazole-4-carbaldehyde (55 mg, 0.239 mmol) in ethanol/methanol (2:1, 15 mL) was allowed to stand a room temperature for 96 h. The solid was filtered off, washed with ether and dried to give the title compound (42 mg, 46%) as a powder. LCMS, m/e 464 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720345B1
Source datasetuspto-grants-2004_04
ORD IDord-531f0664b11147d1ac19ab346432fe4e
Source noteuspto-grants-2004_04