돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601993생성일: 2026년 10월 24일

Triethylamine → N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamide

https://huagongshe.com/ko/reaction/601993

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(S)-(+)-1-CyclohexylethylamineHCID 5325951—
반응물3-Fluoro-4-(2-propynyloxy)benzoyl chlorideHCID 57445684—
용매Ethyl AcetateHCID 8857—
생성물N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamideHCID 5770121086.4%

반응 단계

To a mixture of 5 ml of ethyl acetate and 0.30 g of 3-fluoro-4-(2-propynyloxy)benzoyl chloride were added 0.22 g of (1S)-1-(cyclohexyl)ethylamine and 0.20 g of triethylamine in order at room temperature. The mixture obtained was stirred at room temperature for 1 hour. Then, ethyl acetate was added to the reaction mixture and the mixture was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was washed with hexane to obtain 0.37 g of N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 37 of the present invention) represented by the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902400B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-2a5bf7b9c734421d8ef49376c9eceadf
출처 메모uspto-grants-2011_03