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1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea → 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985545 | — |
| 触媒 | Lindlars catalyst | HCID 131709914 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea | HCID 86588973 | 41% |
反応手順
A suspension of 1-(6-phenylacetylenyl-2-benzothiazolyl)-3-ethylurea (0.032 g, 83% purity by weight, 0.083 mmol) and Lindlar catalyst (0.030 g, 5% weight purity, 0.012 mmol, 0.15 eq) in 2 mL ethanol was purged with nitrogen gas, followed by bubbling of hydrogen gas. It was stirred under hydrogen atmosphere for about 36 hours. The mixture was taken up in 10 mL MeOH, filtered, concentrated, and purified by preparative TLC to give 0.011 g (41%) of the desired compound. LC/MS 324 (M+1); LC retention time 2.84 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091227B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-b034843c1eae49b58ee346d1b1960c87 |
| 出典メモ | uspto-grants-2006_08 |