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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| 반응물 | N-(2,6-dichloropyrimidin-4-yl)acetamide | HCID 4713752 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(6-Acetylamino-2-chloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 86618545 | 8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07674804B2 |
|---|
| 출처 데이터셋 | uspto-grants-2010_03 |
|---|
| ORD ID | ord-22e7bb4d6fe3415493de46eff9ebd583 |
|---|
| 출처 메모 | uspto-grants-2010_03 |
|---|