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HRID 660543作成日:2026年10月27日

Imidazole → 5-(2-Benzyloxy-4-iodomethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one

https://huagongshe.com/reaction/660543

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物IodineHCID 807—
反応物TriphenylphosphineHCID 11776—
反応物5-(2-Benzyloxy-4-hydroxymethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756654—
溶媒DichloromethaneHCID 6344—
生成物5-(2-Benzyloxy-4-iodomethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756809—

反応条件

温度0 °C

反応手順

To a 0° C. slurry of resin-bound PPh3 (850 mg, 2.5 mmol) in CH2Cl2 (10 mL) in a pressure vessel is added imidazole (200 mg, 2.8 mmol) and iodine (650 mg, 2.5 mmol). The mixture is vigorously stirred at 0° C. for 30 min. To the mixture is added a solution of 5-(2-benzyloxy-4-hydroxymethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (550 mg, 1.2 mmol) in CH2Cl2 (10 mL) dropwise. The vessel is sealed and heated to 45° C., with stirring, for 2 h. The reaction is allowed to cool to RT and the mixture is filtered through a plug of cotton to remove the resin. The organic solution is washed with sat. Na2SO3 and brine, then dried over MgSO4. The solvent is removed under reduced pressure to afford the title compound as a white solid which is used in the next step without further purification: (M+H)+=576.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08084448B2
出典データセットuspto-grants-2011_12
ORD IDord-e414390b6c7b4237afa1d6e317f7f2ea
出典メモuspto-grants-2011_12