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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15617생성일: 2026년 10월 25일

Cyclohexylamine → N-lauroyl-L-valine cyclohexylamide

https://huagongshe.com/reaction/15617

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexylamineHCID 7965—
반응물N-(1-Oxododecyl)-L-valineHCID 26658—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N-Hydroxysuccinimide hydrateHCID 18987794—
용매ChloroformHCID 6212—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물N-lauroyl-L-valine cyclohexylamideHCID 1152376444%

반응 단계

61 mg (0.20 mmol) of N-lauroyl-L-valine and 39 mg (0.26 mmol) of N-hydroxysuccinimide monohydrate were dissolved into 3.0 mL of dried chloroform. 50 mg (0.26 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added thereto under argon atmosphere and in the ice bath, and stirred at 0° C. for 3 hours. 35 μL of triethylamine and 35 μL of cyclohexylamine were added thereto and stirred at room temperature overnight. Then, 20 mL of ethyl acetate was added thereto and washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate. The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure. The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1) to obtain 34 mg of N-lauroyl-L-valine cyclohexylamide (0.089 mmol, yield 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732637B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-73b79f894c14436c94e4a13255d20079
출처 메모uspto-grants-2010_06