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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243813생성일: 2026년 10월 24일

Diisopropylethylamine → 1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea

https://huagongshe.com/ko/reaction/243813

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물L-Tartaric acidHCID 444305—
반응물rac-(1R,2S)-2-amino-2,3-dihydro-1H-inden-1-olHCID 11008081—
반응물2,2,2-Trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamateHCID 68107458—
용매AcetonitrileHCID 6342—
생성물1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)ureaHCID 6810780451%

반응 조건

온도110 °C

반응 단계

To a solution of 2,2,2-trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamate (0.086 g, 0.203 mmol) and (1S,2R)-2-amino-2,3-dihydro-1H-indene-1-ol.L-tartaric acid salt (0.067 g, 0.223 mmol) in acetonitrile (0.8 mL), N,N-diisopropylethylamine (0.058 mL, 0.333 mmol) was added, the mixture was stirred overnight at 110° C. The reaction mixture was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=10/90-60/40) to obtain 0.044 g of the captioned compound (51% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653304B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-bcc932fdcde14f20ba571ba2466d1d37
출처 메모uspto-grants-2014_02