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Dimethylformamide → N3-[amino(imino)methyl]-N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| 反応物 | N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide | HCID 131737010 | — |
| 生成物 | N3-[amino(imino)methyl]-N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide | HCID 131737012 | — |
反応手順
N3-methyl-N-[4-(triphenylphosphonio)butyl]-β-alaninamide bromide (980 mg, 2.0 mmol) was dissolved in N,N-dimethylformamide (2 mL). The resultant solution was treated with 1H-pyrazole-1-carboximidamide hydrochloride (315 mg, 2.15 mmol) and N,N-diisopropylethylamine (0.39 mL, 2.26 mmol). The reaction was stirred overnight at room temperature. More 1H-pyrazole-1-carboximidamide hydrochloride and N,N-diisopropylethylamine can be added to effect further conversion. The reaction mixture in N,N-dimethylformamide was used without work-up in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434753B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-fb4e85a7232447ad8e7d394428661f39 |
| 出典メモ | uspto-grants-2016_09 |