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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409356Generated: October 29, 2026

Beta-Alanine → HCID 76698629, compound

https://huagongshe.com/reaction/409356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantHCID 16768839HCID 16768839—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 57994057HCID 57994057—
SolventAcetic AcidHCID 176—
ProductHCID 76698629HCID 76698629—

Reaction Conditions

Temperature170 °C

Reaction Steps

To a mixture of 2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid (0.055 g, 0.207 mmol) and 5-(3,4-dichloro-phenyl)thiophene-2-carbaldehyde (0.050 g, 0.207 mmol) in acetic acid 5 mL is added β-alanine (1.8 mg, 0.021 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, 0.123 mmol, red solid) is obtained by column chromatography using MeOH/DCM, 2-7% ration solvent system. 1H-NMR (CDCl3/CD3OD/300 MHz): 7.84 (d, J=2.1 Hz, 1H), 7.60 (dd, J=8.7, 2.4 Hz, 1H), 7.44 (d, J=2.7 Hz, 1H), 7.17 (m, 6H), 6.85 (m, 1H), 6.42 (s, 1H), 5.61 (dd, J=11.1, 5.4 Hz, 1H), 3.66 (m, 1H), 3.53 (m, 1H). MS (ES−, m/z): 585.3 (M−, 100.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759384B2
Source datasetuspto-grants-2014_06
ORD IDord-6e752bc0d5214a93b845ce0181428ac5
Source noteuspto-grants-2014_06