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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56377생성일: 2026년 10월 24일

Cesium carbonate → tert-butyl ((1S,2R)-2-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)cyclohexyl)carbamate

https://huagongshe.com/ko/reaction/56377

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-butyl N-[(1S,2S)-2-aminocyclohexyl]carbamateHCID 1514391—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물2-Chloro-6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolineHCID 89921772—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylacetamideHCID 31374—
생성물tert-butyl ((1S,2R)-2-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)cyclohexyl)carbamateHCID 11804343945.3%

반응 조건

온도125 °C

반응 단계

A mixture of 2-chloro-6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazoline (0.1 g, 0.27 mmol), tert-butyl ((1S,2S)-2-aminocyclohexyl)carbamate (75 mg, 0.35 mmol), Cs2CO3 (176 mg, 0.54 mmol), X-Phos (13 mg, 0.027 mmol) and Pd2dba3 (12.5 mg, 0.013 mmol) in DMA (1.8 mL) was degassed with N2 for 5 mins and heated in a microwave reactor at 125° C. for 30 mins. The mixture was cooled to room temperature, filtered through celite and washed with water followed by saturated brine solution. The residue was purified by silica gel column chromatography to afford tert-butyl ((1S,2R)-2-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)cyclohexyl)carbamate (67 mg, 45%). MS (ES+) C27H32Cl2N4O4 requires: 546, found: 547 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434700B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-bc6fea8b125d4e8ebe4d6b090353c70d
출처 메모uspto-grants-2016_09