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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409359Generated: October 29, 2026

Beta-Alanine → HCID 75038130, compound

https://huagongshe.com/reaction/409359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
Reactant5-(4-Fluorophenyl)-2-thiophenecarboxaldehydeHCID 3577778—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 57994057HCID 57994057—
SolventAcetic AcidHCID 176—
ProductHCID 75038130HCID 75038130—

Reaction Conditions

Temperature170 °C

Reaction Steps

To a mixture of 2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid (0.100g, 0.378 mmol) and 5-(4-fluorophenyl)thiophene-2-carbaldehyde (0.078 g, 0.378 mmol) in acetic acid 5 mL is added β-alanine (3.37 mg, 0.038 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 (0.125 g, 0.276 mmol, red solid) is obtained by column chromatography using MeOH/DCM, 2-7% ration solvent system. 1H-NMR (CD3OD/300 MHz): 7.71 (m, 2H), 7.52 (d, J=4.5 Hz, 1H), 7.43 (d, J=4.5 Hz, 1H), 7.16 (m, 7H), 6.69 (s, 1H), 5.66 (dd, J=11.4, 5.1 Hz, 1H), 3.69 (dd, J=14.4, 11.7 Hz, 1H), 3.51 (dd, J=10.5, 5.1 Hz, 1H). MS (ES−, m/z): 451.4 (M−−1, 45.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759384B2
Source datasetuspto-grants-2014_06
ORD IDord-b5bb94cb8de74c26a226a84f1f199a74
Source noteuspto-grants-2014_06