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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409361Generated: October 30, 2026

Beta-Alanine → HCID 57994046, compound

https://huagongshe.com/reaction/409361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
Reactant5-(4-bromophenyl)thiophene-2-carbaldehydeHCID 3578056—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 57994057HCID 57994057—
SolventAcetic AcidHCID 176—
ProductHCID 57994046HCID 57994046—

Reaction Conditions

Temperature170 °C

Reaction Steps

To a mixture of 2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid (0.053 g, 0.199 mmol) and 5-(4-bromophenyl)thiophene-2-carbaldehyde (0.050 g, 0.199 mmol) in acetic acid 5 mL is added β-alanine (1.8 mg, 0.020 mmol) and heat to 170° C. for 30 min under microwave irradiation. The resulting reaction mixture is cooled down and the solvent is removed. The pure product (0.060 g, 0.120 mmol, red solid) is obtained by column chromatography using MeOH/DCM, 2-7% ration solvent system. 1H-NMR (CD3OD/300 MHz): 7.83 (dm, J=9.0 Hz, 2H), 7.44 (dm, J=9.3 Hz, 2H), 7.17 (m, 5H), 7.03 (s, 2H), 6.47 (s, 1H), 5.64 (d, J=8.7 Hz, 1H), 3.69 (m, 1H), 3.49 (m, 1H). MS (ES−, m/z): 495.2 (M−, 80.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759384B2
Source datasetuspto-grants-2014_06
ORD IDord-dda2fc13f046444b8f9e49313082ab67
Source noteuspto-grants-2014_06