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HRID 1770537作成日:2026年10月25日

Piperonyl alcohol → 1-(benzo[d][1,3]dioxol-5-ylmethyl)-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dione

https://huagongshe.com/reaction/1770537

反応式

関与物質

役割名称HCID仕込み量
反応物Piperonyl alcoholHCID 10322—
反応物3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dioneHCID 57422424—
生成物1-(benzo[d][1,3]dioxol-5-ylmethyl)-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dioneHCID 5794493619%

反応手順

Prepared as in example 10-35 from 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dione (example 10-1) and benzo[d][1,3]dioxol-5-ylmethanol. Yield: 19%. 1H NMR (DMSO, 400 MHz): δ2.143 (s, 3H), 2.408 (s, 3H), 3.977 (s, 2H), 4.440 (s, 2H), 5.202 (s, 2H), 6.003 (s, 2H), 6.897 (m, 3H), 7.788 (s, 1H), 8.181 (s, 1H). MS M+H calculated 410.1. Found 410.1. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.07 uM.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09247759B2
出典データセットuspto-grants-2016_02
ORD IDord-b66143d3eeb44a099d565ee5c0e18440
出典メモuspto-grants-2016_02