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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548170Generated: October 28, 2026

Phenethyl bromide → HCID 57422489, compound

https://huagongshe.com/reaction/548170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
Reactant3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dioneHCID 57422424—
ProductHCID 57422489HCID 5742248937%

Reaction Steps

Prepared as in example 10-52 from 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dione (example 10-1) and phenethylbromide. Yield: 37%. 1H NMR (DMSO-d6, 400 MHz): δ2.11 (s, 3H), 2.38 (s, 3H), 2.83 (t, J=6.4 Hz, 2H), 3.55 (t, J=7.4 Hz, 2H), 4.03 (s, 2H), 5.17 (s, 2H), 7.18-7.30 (m, 5H), 7.73 (s, 1H), 8.13 (s, 1H). MS M+H calculated 380.2; found 380.1. Melting point: 95-96° C. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.14 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939671B2
Source datasetuspto-grants-2011_05
ORD IDord-e72f5c13dbaf484bafea79e4a28f53da
Source noteuspto-grants-2011_05