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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658666Generated: October 30, 2026

Anisole → HCID 57422418, compound

https://huagongshe.com/reaction/658666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 57422419HCID 57422419—
SolventDichloromethaneHCID 6344—
ProductHCID 57422418HCID 5742241862%

Reaction Steps

1-benzyl-5-(2,4-dimethoxybenzyl)-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1,3,5-triazinan-2-one (example 9-6a) (44 mg, 0.09 mmol), anisole (9 mg, 0.09 mmol), and 50% trifluoroacetic acid/dichloromethane solution (1 mL) in dichloromethane (1 mL) were stirred at room temperature for 2 hours. The reaction was concentrated, quenched with saturated sodium bicarbonate (50 mL), extracted with ethyl acetate (2×, 50 mL) and washed with brine (50 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. Purification by silica column chromotography (100% to 90% dichloromethane in methanol: 30 minute gradient) afforded 1-benzyl-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1,3,5-triazinan-2-one (19 mg, 62%) as a white solid. LC/MS; [M+H] calculated for C19H22N6O2; expected 367.18; found 367.20. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 5.84 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076491B2
Source datasetuspto-grants-2011_12
ORD IDord-6a99c86725e24b7cb10023fd2044890c
Source noteuspto-grants-2011_12