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HRID 240281作成日:2026年10月25日
(3R)-3-Aminopiperidine, 3-BOC protected → (R)-tert-butyl 1-(4-(2-bromo-5-fluorobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate
https://huagongshe.com/reaction/240281
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (3R)-3-Aminopiperidine, 3-BOC protected | HCID 1514172 | — |
| 反応物 | 4-(2-bromo-5-fluorobenzyl)-6-methyl-3-(methylthio)-1,2,4-triazin-5(4H)-one | HCID 58328530 | — |
| 生成物 | (R)-tert-butyl 1-(4-(2-bromo-5-fluorobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate | HCID 58328539 | — |
反応手順
The mixture of 4-(2-bromo-5-fluorobenzyl)-6-methyl-3-(methylthio)-1,2,4-triazin-5(4H)-one (17, 180 mg, 0.523 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (208 mg, 1.04 mmol) was ground for 5 min and then heated in a tube under nitrogen atmosphere at 135° C. for 13 h. The mixture was separated by silica gel column, and eluted with 10-50% ethyl acetate in petroleum ether to give (R)-tert-butyl 1-(4-(2-bromo-5-fluorobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate (18). MS: m/z, 496 (100%, M+1), 498 (100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08648073B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-4956c51ad41e4fdfa7aa5931f8e62f3e |
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| 出典メモ | uspto-grants-2014_02 |
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