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Acetic Acid → Ethyl 5-[2-[(4-chlorophenyl)amino]-1-(4-methylpiperazin-1-yl)-2-oxoethyl]thiophene-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 1-Methylpiperazine | HCID 53167 | — |
| 反応物 | 4-Chlorophenyl isocyanide | HCID 74670 | — |
| 反応物 | Ethyl 5-formylthiophene-2-carboxylate | HCID 10797570 | — |
| 溶媒 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 生成物 | Ethyl 5-[2-[(4-chlorophenyl)amino]-1-(4-methylpiperazin-1-yl)-2-oxoethyl]thiophene-2-carboxylate | HCID 57611900 | — |
反応手順
Ethyl 5-formylthiophene-2-carboxylate (0.50 g, 2.71 mmol) was made 2.25 M in anhydrous trifluoroethanol and to this stirring solution was added N-methylpiperazine (0.33 g, 3.26 mmol), 1-chloro-4-isocyanobenzene (0.45 g, 3.26 mmol) and acetic acid (0.20 g, 3.26 mmol). The resulting mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated in vacuo then purified by MPLC to give the desired product. MS: cal'd 422, 424 (MH+), exp 422, 424 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08168658B2 |
| 出典データセット | uspto-grants-2012_05 |
| ORD ID | ord-540ccf93ef494caea6b5ba8d356c35ac |
| 出典メモ | uspto-grants-2012_05 |