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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57614생성일: 2026년 10월 25일

Cesium carbonate → Tert-butyl 3,3-difluoro-5-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/57614

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물TricyclohexylphosphineHCID 75806—
반응물(4-(Morpholin-4-yl)phenyl)boronic acidHCID 2795359—
반응물Tert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylateHCID 86717382—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Water 1,2-dimethoxyethaneHCID 18180031—
생성물Tert-butyl 3,3-difluoro-5-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)piperidine-1-carboxylateHCID 71113804—

반응 조건

온도160 °C

반응 단계

A mixture of tert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylate (206 mg, 0.5 mmol), 4-morpholinophenylboronic acid (207 mg, 1.0 mmol), tri(cyclohexyl)phosphine (56 mg, 0.2 mmol), Pd2(dba)3 (91 mg, 0.1 mmol) and Cs2CO3 (325 mg, 2.0 mmol) in dimethoxyethane/H2O was sealed in a microwave reaction tube and stirred at 160° C. for 80 minutes in a microwave reactor. The mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was purified by chromatography to give the title compound. MS (m/z): 541 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434726B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-748e2ead300e489bbc91e6741afdf325
출처 메모uspto-grants-2016_09