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HRID 1952756作成日:2026年10月25日

Formaldehyde → 4-allyl-2-[4-(1,4-benzodioxan-5-yl)piperazin-1-ylmethyl]-5-(3-pyridyl)-1,2,4-triazole-3(2H,4H)-thione

https://huagongshe.com/reaction/1952756

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物EltoprazineHCID 65853—
反応物4-Allyl-5-pyridin-3-yl-4H-[1,2,4]triazole-3-thiolHCID 758288—
溶媒tert-ButanolHCID 6386—
生成物4-allyl-2-[4-(1,4-benzodioxan-5-yl)piperazin-1-ylmethyl]-5-(3-pyridyl)-1,2,4-triazole-3(2H,4H)-thioneHCID 86755722—

反応手順

A mixture of 1-(1,4-benzodioxan-5-yl)piperazine (1 g; prepared in a similar manner to that described in Example 2), 4-allyl-5-(3-pyridyl)-1,2,4-triazole-3(2H,4H)-thione (1 g), 37-40% aqueous formaldehyde solution (0.5 ml) and t-butanol (60 ml) was stirred at ambient temperature for 30 minutes, heated under reflux for 15 minutes, then the solvent was removed in vacuo. The residue was triturated with a 1:1 mixture of cyclohexane and ether (40 ml), and the resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 4-allyl-2-[4-(1,4-benzodioxan-5-yl)piperazin-1-ylmethyl]-5-(3-pyridyl)-1,2,4-triazole-3(2H,4H)-thione as a white solid (0.62 g), m.p. 122-127° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06114334
出典データセットuspto-grants-2000_09
ORD IDord-70b63dc3274e4ac28a5f8d468fbf25e5
出典メモuspto-grants-2000_09