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HRID 1008作成日:2026年10月24日

Hydrochloric Acid → 4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine

https://huagongshe.com/ja/reaction/1008

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
反応物MagnesiumHCID 5462224—
反応物4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridineHCID 19693951—
溶媒Diethyl EtherHCID 3283—
生成物4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridineHCID 67671140—

反応手順

A Grignard solution is prepared from 1.2 g of magnesium and 12.9 g of 90% strength 4-tert-butylbenzyl bromide in 100 ml of abs. ether. 2.9 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine in 50 ml of absolute THF are added dropwise to this solution. After 17 hours at room temperature it is acidified with 25 ml of 2N HCl, the mixture is extracted several times with ethyl acetate and the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution. Purification is carried out by column chromatography on silica gel using ethyl acetate to which increasing amounts of methanol are added.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723450
出典データセットuspto-grants-1998_03
ORD IDord-77b579259b0e47c2ac2dc691717deb93
出典メモuspto-grants-1998_03