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Benzaldehyde → 2,3,5,6,7,8-Hexahydro-2-phenyl-3-(2-thienyl)thiazolo-[3,2-a][1,3]diazepin-3-ol methanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 1,3-Diazepane-2-thione | HCID 736589 | — |
| 反応物 | 2-Thienyl-alpha-hydroxybenzyl ketone | HCID 54002001 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2,3,5,6,7,8-Hexahydro-2-phenyl-3-(2-thienyl)thiazolo-[3,2-a][1,3]diazepin-3-ol methanesulfonate | HCID 20528326 | — |
反応手順
A mixture of 9.2 ml. of thiophene-2-carboxyaldehyde, 8 g. of potassium cyanide and 10.1 ml. of benzaldehyde in 100 ml. of 65% ethanol is reacted as described in Example 20, giving 6.2 g. of 2-thienyl-α-hydroxybenzyl ketone. A 4.36 g. portion of this ketone is reacted with methanesulfonyl chloride as described in Example 20, giving 3.2 g. of the methanesulfonate ester. A 2.64 g. portion of this ester and 1.30 g. of hexahydro-2H-1,3-diazepine-2-thione in 100 ml. of acetone are allowed to stand 48 hours, the solid is collected, washed with ether and dried in vacuo, giving 2.8 g. of the desired product, m.p. 149°-151° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04344954 |
| 出典データセット | uspto-grants-1982_08 |
| ORD ID | ord-34472b1a55034bc2a3b0726c4608e611 |
| 出典メモ | uspto-grants-1982_08 |