化工社化工社 化学情報印刷レポート · 研究参考用
Dimethylformamide → Tert-butyl 4-(3-chloropyrazin-2-yl)-3-methylpiperazine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 2,3-Dichloropyrazine | HCID 78575 | — |
| 反応物 | tert-Butyl 3-methylpiperazine-1-carboxylate | HCID 2756810 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Tert-butyl 4-(3-chloropyrazin-2-yl)-3-methylpiperazine-1-carboxylate | HCID 21908991 | 45% |
反応手順
3-Methyl-piperazine-1-carboxylic acid tert-butyl ester (5.0 g, 25 mmol), 2,3-dichloropyrazine (1.3 mL, 12.5 mmol), and DMF (5.0 mL) were combined and heated to 100 C overnight with stirring. The reaction mixture was poured into H2O and extracted with EtOAc (3×). The combined EtOAc extractions were washed with sat'd NaHCO3 (2×), sat's NaCl (1×), dried (Na2SO4), and concentrated in vacuo. The crude product was purified by column chromatography (4:1 hexanes:EtOAc) to give 1.76 g (45%) of 3′-chloro-2-methyl-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester. 1H NMR (CDCl3) 8.08 (d, 1H), 7.86 (d, 1H), 4.22-3.76 (complex m, 3H), 3.48-3.17 (complex m, 4H), 1.48 (s, 9H), 1.19 (d, 3H) ppm. LC-MS (MH+)=257 (-t-butyl).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08013156B2 |
| 出典データセット | uspto-grants-2011_09 |
| ORD ID | ord-8ac4cfe6e9454662b3402a2c0b3b48f0 |
| 出典メモ | uspto-grants-2011_09 |