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Potassium Hydroxide → 1-(7-Acetylenyl-2-benzothiazolyl)-3-ethylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | N,N-dimethylformamide methanol | HCID 21901440 | — |
| 反応物 | 1-(7-Trimethylsilylacetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985538 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | 1-(7-Acetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985650 | 15.3% |
反応手順
A mixture of 1-(7-trimethylsilylacetylenyl-2-benzothiazolyl)-3-ethylurea 2 (0.050 g, 0.16 mmol) and 1M aqueous KOH solution (0.16 mL, 0.16 mmol, 1.0 eq) in 1.5 mL of 2/1 mixture of DMF/MeOH was stirred at room temperature for about 2 hours. The mixture was taken up in 10 mL MeOH and the precipitation was filtered off. The mother liquid was concentrated and purified by prep HPLC to give the desired compound 0.006 g (15%). LC/MS 246 (M+1); LC retention time 2.77 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-8abe128357e5495cb8583bed1bcfdda2 |
| 出典メモ | uspto-grants-2006_08 |