関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1H-1,2,4-Triazole, 1-methyl- | HCID 22459 | — |
| 反応物 | N-methoxy-N-methylcarbamoyl chloride | HCID 2734926 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-methoxy-N,1-dimethyl-1H-1,2,4-triazole-5-carboxamide | HCID 86658057 | 65% |
反応手順
A mixture of 1-methyl-1H-1,2,4-triazole (3.15 mL, 55.56 mmol) and methoxy(methyl)carbamic chloride (7.55 g, 61.11 mmol) in acetonitrile (60 mL) was cooled in an ice water bath before addition of TEA (8.52 mL, 61.11 mmol). The mixture was allowed to slowly warm to room temperature and was then stirred overnight. The material was diluted with ether and solids were filtered and rinsed well with ether. The filtrate was concentrated and the residue was taken up in ether. Insoluble solids were filtered off and rinsed well with additional ether. The filtrate was concentrated to give and oil that was chromatographed on silica gel (100% CH2Cl2 followed by gradient elution to 40% EtOAc in CH2Cl2) to afford product as an oil that slowly solidified. 6.13 g (65% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08658641B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-40a9817998df41a58e92a8f25b73ce8c |
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| 出典メモ | uspto-grants-2014_02 |
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