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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677382생성일: 2026년 10월 25일

1-Methylcyclohexane-1-carboxaldehyde → (1-methyl-cyclohexyl)-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-methanol

https://huagongshe.com/reaction/1677382

반응식

참여 물질

역할이름HCID투입량
반응물1-Methylcyclohexane-1-carboxaldehydeHCID 11137168—
반응물7-iodo-5-triisopropylsilanyl-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazineHCID 59540525—
반응물HCID 178461733HCID 178461733—
용매TetrahydrofuranHCID 8028—
생성물(1-methyl-cyclohexyl)-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-methanolHCID 5954070745.3%

반응 단계

A solution of 7-iodo-5-triisopropylsilanyl-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine (247 mg, 0.435 mmol) in anhydrous tetrahydrofuran (5 ml) was cooled to −78° C. and treated with iPrMgCl—LiCl (1M in tetrahydrofuran, 0.87 ml, 0.87 mmol) dropwise. The reaction mixture was allowed to stir for 20 minutes, and then 1-methyl-cyclohexanecarbaldehyde (219 mg, 1.74 mmol) was added rapidly. The reaction mixture was allowed to stir at −78° C. for 1 hour and then room temperature for 1 hour. The reaction mixture was partitioned between EtOAc/saturated aqueous. NH4Cl. The organic layers were collected, dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography using 15-100% EtOAc in hexanes as eluant to provide 81 mg (45%) of (1-methyl-cyclohexyl)-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-methanol as a pale yellow solid. M+H=412.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008298B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-93ac8c2e43d14235a5e73b9db74e3916
출처 메모uspto-grants-2011_08