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HRID 1833713作成日:2026年10月25日

Ethanol → 1-(2-[6-Methylnicotinoyl]-1-methylvinylamino)-3-(p-[4-methoxybutoxy]-phenoxy)-propan-2-ol

https://huagongshe.com/reaction/1833713

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物1-(6-Methylpyridin-3-yl)butane-1,3-dioneHCID 20212814—
反応物HCID 20352683HCID 20352683—
溶媒Formic AcidHCID 284—
生成物1-(2-[6-Methylnicotinoyl]-1-methylvinylamino)-3-(p-[4-methoxybutoxy]-phenoxy)-propan-2-olHCID 7061868389%

反応手順

54.0 g of 1-(p-[4-methoxybutoxy]-phenoxy)-3-aminopropan-2-ol ##STR76## 37.3 g of 6-methylnicotinoyl-acetone ##STR77## 400 ml of ethanol and 0.1 ml of formic acid are heated to 50° for 1 hour and stirred at room temperature for a further 20 hours. Filtration gives 61.3 g of 1-(2-[6-methylnicotinoyl]-1-methylvinylamino)-3-(p-[4-methoxybutoxy]-phenoxy)-propan-2-ol ##STR78## Melting point: 143°-145°. A further 15.0 g of the same substance can be obtained from the filtrate. Yield: 89% of theory.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04066768
出典データセットuspto-grants-1978_01
ORD IDord-e803bd29ad03488d9c7084cea1930d69
出典メモuspto-grants-1978_01