戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 219709作成日:2026年10月26日

Sodium Iodide → (S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl ester

https://huagongshe.com/reaction/219709

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物(R)-(-)-1-acetoxy-3-bromo-2-methyl-propaneHCID 10420167—
反応物2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidineHCID 66673390—
溶媒DimethylformamideHCID 6228—
生成物(S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl esterHCID 131729779102.9%

反応条件

温度95 °C

反応手順

3.87 g of 2-tert-butyl-4-cyclobutyl-6-piperazin-1-yl-pyrimidine (14.1 mmol) were stirred in 30 ml of dimethylformamide at room temperature. 3.18 g of triethylamine (63.1 mmol), 0.235 g of sodium iodide (1.57 mmol), 2.96 g of (R)-(−)-1-acetoxy-3-bromo-2-methyl-propane (15.2 mmol) were added and the reaction mixture was stirred for 5 h at 95° C. The dimethylformamide was evaporated under reduced pressure. The residue was partitioned between 100 ml of dichloromethane and 100 ml of water. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure to give a brownish oil (5.64 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202868B2
出典データセットuspto-grants-2012_06
ORD IDord-8ad93d4589f643a19d73bbb7382181e8
出典メモuspto-grants-2012_06