돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430804생성일: 2026년 10월 24일

1-Phenylcyclopentanecarboxylic acid → (s)-1-Phenyl-cyclopentanecarboxylic acid [2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-amide

https://huagongshe.com/ko/reaction/430804

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenylcyclopentanecarboxylic acidHCID 66167—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물(S)-2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamideHCID 15517727—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물(s)-1-Phenyl-cyclopentanecarboxylic acid [2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-amideHCID 989212445%

반응 조건

온도0 °C

반응 단계

1-Phenyl-1-cyclopentanecarboxylic acid (0.171 g, 0.899 mmol) was dissolved in dry DMF (3 mL) under a nitrogen atmosphere and cooled to 0° C. in an ice-water bath. To this solution were added in succession N,N-diisopropylethylamine (0.310 mL, 1.80 mmol) and solid O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.341 g, 0.899 mmol, Novabiochem, La Jolla, Calif.). The resulting reaction mixture was stirred at 0° C. for 30 minutes, (S)-2-Amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide (0.293 g, 0.899 mmol) was then added. After an additional 60 minutes stirring at 0° C., the reaction mixture was mixed with 60 mL of diethyl ether. The resulting mixture was successively washed with 5% aqueous HCl solution, brine, saturated aqueous NaHCO3 solution and brine, and was dried over Na2SO4. The solution was concentrated in vacuo, and an oil was obtained. The crude residue was purified by chromatography (silica gel, 60% ether in hexanes) to give the title compound as a white foam (0.20 g, 45%); mp 40-50° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323243B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-13f94147e9424f0caa6371d873033357
출처 메모uspto-grants-2001_11