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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12362생성일: 2026년 10월 23일

N-(2-Aminoethyl)piperidine → 8-Cyclohexyl-5-oxo-2-(2-piperidin-1-yl-ethylamino)-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/12362

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Aminoethyl)piperidineHCID 33944—
반응물8-Cyclohexyl-2-methanesulfonyl-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl esterHCID 25223482—
생성물8-Cyclohexyl-5-oxo-2-(2-piperidin-1-yl-ethylamino)-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl esterHCID 68583945—

반응 단계

Using the procedure outlined in Example 28 Step F, the title compound was prepared from 2-piperidin-1-yl-ethylamine and 8-cyclohexyl-2-methanesulfonyl-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (25 mg, 0.06 mmol). 8-Cyclohexyl-5-oxo-2-(2-piperidin-1-yl-ethylamino)-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester was obtained as a white solid (20 mg, 80%). Mass Spectrum (LCMS, ESI pos.) Calcd. For C23H33N5O3: 428.26 (M+H). Found: 428.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728003B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9ce6fc1cc68d47d58102841dd0dba082
출처 메모uspto-grants-2010_06