戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 578714作成日:2026年10月25日

Cesium carbonate → tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-phenylquinazolin-4-yl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/578714

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Phenylboronic AcidHCID 66827—
反応物tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-iodoquinazolin-4-yl]amino}piperidine-1-carboxylateHCID 66762696—
触媒HCID 178454917HCID 178454917—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-phenylquinazolin-4-yl]amino}piperidine-1-carboxylateHCID 66763488—

反応手順

Combined phenylboronic acid (16.18 mg; 0.13 mmol; 1.20 eq.), tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-iodoquinazolin-4-yl]amino}piperidine-1-carboxylate (55.00 mg; 0.11 mmol; 1.00 eq.), and bis(tri-tert-butylphosphoranyl)palladium (5.67 mg; 0.01 mmol; 0.10 eq.) in a microwave tube. Then added THF (0.70 ml) followed by cesium carbonate (0.22 ml; 2.00 M; 0.44 mmol; 4.00 eq.). Heated reaction in the microwave at 130 deg C. for 20 minutes. LCMS: M+1=448 major peak (266 present). Concentrated reaction. Purified by silica gel chromatography (Biotage; 10 g column; 15 mL/min; 1-10% MeOH/CH2Cl2). Concentrated product to give an oil. LCMS: M+1=448 major peak.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040560B2
出典データセットuspto-grants-2015_05
ORD IDord-1a53dd870e244fd2bbae339303581dfa
出典メモuspto-grants-2015_05