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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658794Generated: October 30, 2026

4-Methoxybenzyl bromide → HCID 53373744, compound

https://huagongshe.com/reaction/658794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl bromideHCID 165021—
Reactant3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-5,5-dimethylimidazolidine-2,4-dioneHCID 59524388—
ProductHCID 53373744HCID 5337374435%

Reaction Steps

Prepared as in Example 12-16 from 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-5,5-dimethylimidazolidine-2,4-dione (Example 12-16a) and 1-(bromomethyl)-4-methoxybenzene. Yield 35%, colorless gel (195 mg, 35%). 1H NMR (DMSO-d6, 400 MHz): □s, 6H), 2.14 (s, 3H), 2.40 (s, 3H), 3.71 (s, 3H), 4.48 (s, 2H), 5.18 (s, 2H) 6.87 (d, J=8.8 Hz, 2H), 7.31 (d, J=8.4 Hz, 2H), 7.80 (s, 1H), 8.18 (s, 1H). MS 424 (MH+). The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.11 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076491B2
Source datasetuspto-grants-2011_12
ORD IDord-09f60059934142c792166a34f6b86eb0
Source noteuspto-grants-2011_12