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HRID 894573作成日:2026年10月24日

Methoxyacetic Acid → 5-(Methoxymethyl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/ja/reaction/894573

反応式

関与物質

役割名称HCID仕込み量
反応物Methoxyacetic AcidHCID 12251—
反応物ThiosemicarbazideHCID 2723789—
溶媒WaterHCID 962—
生成物5-(Methoxymethyl)-1,3,4-thiadiazol-2-amineHCID 660844—

反応手順

Addition of phosphonyl chloride to a mixture of thiosemicarbazide and methoxyacetic acid at 60°-95° and working up of the product yields 5-amino-2-methoxymethyl-(1,3,4)-thiadiazole, m.p. 177°-179° (from water). When this compound is diazotised and treated with cuprous bromide 5-bromo-2-methoxymethyl-(1,3,4)-thiadiazole results and reaction of this bromo compound with zinc dust in acetic acid at room temperature yields 2-methoxymethyl-(1,3,4)-thiadiazole, m.p. 30.5°-32°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284640
出典データセットuspto-grants-1981_08
ORD IDord-8c26dff5f7bc496696e4daaa46a79d7e
出典メモuspto-grants-1981_08