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HRID 2426557作成日:2026年10月25日
4-Amino-1-Boc-piperidine → 4-(6-Acetylamino-2-chloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/2426557
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| 反応物 | N-(2,6-dichloropyrimidin-4-yl)acetamide | HCID 4713752 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(6-Acetylamino-2-chloro-pyrimidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 86618545 | 8% |
反応手順
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): δ1.33-1.45 (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]+.
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-a92c7e1cbdad4809a70d022c074e4a5f |
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| 出典メモ | uspto-grants-2011_06 |
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