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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
반응물MagnesiumHCID 5462224—
반응물4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridineHCID 19693951—
용매Diethyl EtherHCID 3283—
생성물4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridineHCID 67671140—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723450
출처 데이터셋uspto-grants-1998_03
ORD IDord-77b579259b0e47c2ac2dc691717deb93
출처 메모uspto-grants-1998_03