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HRID 67235作成日:2026年10月25日

Benzaldehyde → 2,3,5,6,7,8-Hexahydro-2-phenyl-3-(2-thienyl)thiazolo-[3,2-a][1,3]diazepin-3-ol methanesulfonate

https://huagongshe.com/reaction/67235

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Potassium CyanideHCID 9032—
反応物Methanesulfonyl chlorideHCID 31297—
反応物1,3-Diazepane-2-thioneHCID 736589—
反応物2-Thienyl-alpha-hydroxybenzyl ketoneHCID 54002001—
溶媒AcetoneHCID 180—
溶媒EthanolHCID 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 methanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04344954
出典データセットuspto-grants-1982_08
ORD IDord-34472b1a55034bc2a3b0726c4608e611
出典メモuspto-grants-1982_08