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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2242974생성일: 2026년 10월 26일

4-Amino-1-Boc-piperidine → 4-(6-Acetylamino-2-chloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2242974

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-1-Boc-piperidineHCID 1268291—
반응물N-(2,6-dichloropyrimidin-4-yl)acetamideHCID 4713752—
용매DimethylformamideHCID 6228—
생성물4-(6-Acetylamino-2-chloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 866185458%

반응 조건

온도130 °C

반응 단계

A mixture of N-(2,6-dichloro-pyrimidin-4-yl)-acetamide (0.7 g, 3.40 mmol, 1.0 equiv; intermediate B1) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (0.82 g, 4.08 mmol, 1.2 equiv) in anhydrous DMF (6 mL) was heated by microwave irradiation to 130° C. for 4 h. Removal of the solvent under reduced pressure and purification with column chromatography on silica eluting with a gradient of heptane/ethyl acetate (3:1→1:1) provided 0.1 g (8%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.33-1.45 (m, 2H), 1.47 (s, 9H), 1.97-2.08 (m, 2H), 2.18 (s, 3H), 2.90-2.99 (m, 2H), 4.01-4.08 (m, 3H), 5.19 (br s, 1H), 7.13 (s, 1H), 8.04 (br s, 1H). MS (ISP): 370.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07674804B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-22e7bb4d6fe3415493de46eff9ebd583
출처 메모uspto-grants-2010_03