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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79202생성일: 2026년 10월 25일

Trifluoroacetic acid → 9-cyclopentyl-N-(5-(1-piperazinylmethyl)-2-pyridinyl)-9 H-pyrido[4',3':4,5]-pyrrolo[2,3-d]pyrimidin-2-amine

https://huagongshe.com/reaction/79202

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물tert-Butyl 4-((6-chloropyridin-3-yl)methyl)piperazine-1-carboxylateHCID 45788993—
반응물9-Cyclopentyl-9H-pyrido[4',3':4,5]pyrrolo[2,3-d]pyrimidin-2-amineHCID 58299585—
생성물9-cyclopentyl-N-(5-(1-piperazinylmethyl)-2-pyridinyl)-9 H-pyrido[4',3':4,5]-pyrrolo[2,3-d]pyrimidin-2-amineHCID 44132903—

반응 단계

Compound 338 was prepared as an off-white solid (TFA salt) from compound 4 and compound 339 using chemistry similar to that described in example 200. 1H NMR (500 MHz, CD3OD) δ ppm 9.68 (1 H, s), 9.35 (1 H, s), 8.68 (2 H, q, J=6.3 Hz), 8.43 (1 H, d, J=1.5 Hz), 8.26 (1 H, dd, J=8.9, 2.1 Hz), 7.88 (1 H, d, J=8.8 Hz), 5.48 (1 H, quin, J=8.7 Hz), 3.78 (2 H, s), 3.27-3.30 (4 H, m), 2.83 (4 H, br. s.), 2.48-2.59 (2 H, m), 2.15-2.31 (4 H, m), 1.83-1.97 (2 H, m). LCMS-ESI (POS), M/Z, M+1: Found 429.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841312B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f0bcf7d094b1467c8629eda6027474fd
출처 메모uspto-grants-2014_09