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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44413생성일: 2026년 10월 24일

Triethylamine → N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/ko/reaction/44413

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-benzyl-N,4-dimethylpiperidin-3-amineHCID 9943889—
반응물HCID 178418725HCID 178418725—
생성물N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 1208482950%

반응 조건

온도100 °C

반응 단계

A solution of 4-chloropyrrolo[2,3-d]pyrimidine (2.4 grams, 15.9 mmol), prepared by the method of Davoll, J. Am. Chem. Soc., 82, 131 (1960), which is incorporated by reference in its entirety, and the product from Method A (1.7 grams, 7.95 mmol) dissolved in 2 equivalents of triethylamine was heated in a sealed tube at 100° C. for 3 days. Following cooling to room temperature and concentration under reduced pressure, the residue was purified by flash chromatography (silica; 3% methanol in dichloromethane) affording 1.3 grams (50%) of the title compound as a colorless oil. LRMS: 336.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541426B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-90ce4c8ad50f4e4aa7af55ff18e28333
출처 메모uspto-grants-2013_09