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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69675생성일: 2026년 10월 24일

Diisopropylethylamine → 7-[4-(4-Chloro-phenyl)-piperazin-1-ylmethyl]-10-oxo-1,3,4,9,10,10a-hexahydro-2,4-a,5,9-tetraaza-phenanthrene-2-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/69675

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(4-Chlorophenyl)piperazine HydrochlorideHCID 3084720—
반응물(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
반응물7-Hydroxymethyl-10-oxo-1,3,4,9,10,10a-hexahydro-2,4-a,5,9-tetraaza-phenanthrene-2-carboxylic acid tert-butyl esterHCID 58324441—
용매PropionitrileHCID 7854—
생성물7-[4-(4-Chloro-phenyl)-piperazin-1-ylmethyl]-10-oxo-1,3,4,9,10,10a-hexahydro-2,4-a,5,9-tetraaza-phenanthrene-2-carboxylic acid tert-butyl esterHCID 5832435582%

반응 조건

온도90 °C

반응 단계

7-Hydroxymethyl-10-oxo-1,3,4,9,10,10a-hexahydro-2,4a,5,9-tetraaza-phenanthrene-2-carboxylic acid tert-butyl ester (22.0 mg, 0.598 mmol) was suspended in propionitrile (1.5 mL) and (cyanomethyl)trimethylphosphonium iodide (174.0 mg, 0.718 mmol) was added followed by N-ethyl-N-isopropylpropan-2-amine (313 ul, 1.794 mmol). To the stirred mixture was then added 1-(4-chlorophenyl)piperazine hydrochloride (139 mg, 0.598 mmol). The reaction was heated to 90° C. with stirring for 16 h. The crude reaction was cooled to room temperature and purified on silica column (24 g, 25% THF in ethyl acetate). The fractions were combined and concentrated to afford 250.9 mg (82%) of the title compound as a brown solid in 80% purity. [M+H] calc'd for C26H33ClN6O3, 513; found, 513.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822470B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7a0e1d4c21f44c328ad1a5ebe00c5468
출처 메모uspto-grants-2014_09