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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474475생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/474475

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Phenylboronic AcidHCID 66827—
반응물tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-iodoquinazolin-4-yl]amino}piperidine-1-carboxylateHCID 66762696—
촉매HCID 178454917HCID 178454917—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-phenylquinazolin-4-yl]amino}piperidine-1-carboxylateHCID 66763488—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637532B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-28fada8295fd419982227fe33fd2e64c
출처 메모uspto-grants-2014_01