돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379395생성일: 2026년 10월 26일

Methanol → N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamide

https://huagongshe.com/reaction/379395

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium HydroxideHCID 14798—
반응물4-{5-[(3,5-Bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl esterHCID 9852319—
용매Ethyl AcetateHCID 8857—
생성물N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamideHCID 1028028687.4%

반응 단계

To a solution of 6.60 g (104 mmol) 4-{5-[(3,5-bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl ester (Example 43) and 8.40 ml (207 mmol) methanol in 50 ml ethyl acetate 14.7 ml (207 mmol) acetyl chloride were added dropwise at 0° C. After 4 h the reaction mixture was diluted with ethyl acetate and treated with 1 N sodium hydroxide solution. The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were dried with sodium sulfate and concentrated to give 5.36 g of crude product. Flash column chromatography afforded 4.86 g (87.4%) of the title compound as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06297375B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-4d0f11e4af2c44a29779c541daeb0e62
출처 메모uspto-grants-2001_10