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HRID 2426550作成日:2026年10月26日
2,4-Dichloro-6-methylpyrimidine → tert-Butyl 4-((2-chloro-6-methylpyrimidin-4-yl)amino)piperidine-1-carboxylate
https://huagongshe.com/reaction/2426550
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4-Dichloro-6-methylpyrimidine | HCID 79471 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | tert-Butyl 4-((2-chloro-6-methylpyrimidin-4-yl)amino)piperidine-1-carboxylate | HCID 60137289 | — |
反応手順
A solution of 2,4-dichloro-6-methyl-pyrimidine (1.25 g, 7.68 mmol, 1.0 equiv; commercially available), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (2.0 g, 10.0 mmol, 1.3 equiv) and N-ethyl diisopropylamine (3.0 mL, 2.3 g, 17.7 mmol, 2.3 equiv) in acetonitrile (16 mL) was heated by microwave irradiation to 160° C. for 20 min. The reaction mixture was concentrated under reduced pressure and the crude material purified by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate providing 1.15 g (46%) of the title compound. 1H NMR (400 MHz, DMSO): δ 1.24-1.31 (m, 2H), 1.40 (s, 9H), 1.80-1.83 (br d, 2H), 2.18 (s, 3H), 2.90 (br s, 2H), 3.87 (br s, 2H), 3.96 (br s, 1H), 6.23 (br s, 1H), 7.68 (d, J=8.0 Hz, 1H). MS (ISP): 327.4 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07968568B2 |
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| 出典データセット | uspto-grants-2011_06 |
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| ORD ID | ord-559b9d5fac5846659fedce01f9bb5a59 |
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| 出典メモ | uspto-grants-2011_06 |
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