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HRID 2107385作成日:2026年10月25日

Formaldehyde → 1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazole

https://huagongshe.com/reaction/2107385

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium HydroxideHCID 14798—
反応物HCID 178480237HCID 178480237—
溶媒EthanolHCID 702—
生成物1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazoleHCID 1403250457.8%

反応手順

A solution of 0.52 g of paraformaldehyde, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole, 15 ml of ethanol and 0.34 ml of 5% aqueous sodium hydroxide was refluxed for 3 hrs. The ethanol was removed in vacuo and the residue diluted with water. The aqueous suspension was extracted with dichloromethane (2x, 50 ml) and the combined extracts were washed with water and dried over anhydrous magnesium sulfate. The dichloromethane was evaporated in vacuo to yield an oil, which crystallized upon standing. The solid was recrystallized twice from ethyl acetate to yield 1.3 g (57.8%) of product, mp 128°-130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04933460
出典データセットuspto-grants-1990_06
ORD IDord-dedefe755fe04af89db7cf37b98d3488
出典メモuspto-grants-1990_06