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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548119Generated: October 26, 2026

1-(Bromomethyl)-2-methoxybenzene → 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1-(2-methoxybenzyl)imidazolidine-2,4-dione

https://huagongshe.com/reaction/548119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-2-methoxybenzeneHCID 40308—
Reactant3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dioneHCID 57422424—
Product3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1-(2-methoxybenzyl)imidazolidine-2,4-dioneHCID 5742244033%

Reaction Steps

Prepared as in example 10-5 from 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dione (example 10-1) and 1-(bromomethyl)-2-methoxybenzene (199 mg, 1 mmol). Yield: 33%. MS M+H calculated 396.1; found 396.1. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.06 uM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939671B2
Source datasetuspto-grants-2011_05
ORD IDord-1c7cac9b9a3c413c8d2a43cb23d65a66
Source noteuspto-grants-2011_05