戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 539715作成日:2026年10月26日

Diisopropylethylamine → Tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/539715

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物TriphosgeneHCID 94429—
反応物4-Amino-2-methylpyridineHCID 728670—
反応物Tert-butyl 4-(3-amino-2-fluorobenzyl)piperazine-1-carboxylateHCID 58919232—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylateHCID 5891922643%

反応条件

温度0 °C

反応手順

To a 0° C. solution of triphosgene (959 mg, 3.24 mmol, 0.35 equiv) in THF (45 mL) was slowly added via cannula a solution of tert-butyl 4-(3-amino-2-fluorobenzyl)piperazine-1-carboxylate (2.86 g, 9.25 mmol, 1.0 equiv) and DIPEA (3.2 mL, 18.5 mmol, 2.0 equiv) in THF (25 mL) over approximately 20 minutes. The solution was stirred for an additional 15 min at 0° C., and 4-amino-2-methylpyridine was then added. After stirring at room temperature for 72 h, the reaction was diluted with EtOAc, washed with aq. satd. NaHCO3 and brine, dried over sodium sulfate, filtered and concentrated in vacuo. Purification by reverse phase preparative HPLC provided tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylate (1.77 g, 43%). LCMS m/z (APCI)=444.3 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871768B2
出典データセットuspto-grants-2014_10
ORD IDord-d2596ea1680648daab9a84ecb290a8dc
出典メモuspto-grants-2014_10