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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2068506생성일: 2026년 10월 27일

Diisopropylethylamine → 1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]

https://huagongshe.com/reaction/2068506

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물p-Chlorocinnamyl chlorideHCID 53728250—
반응물1-Methanesulfonyl-5-chloro-spiro[indoline-3,3'-pyrrolidine]HCID 58137339—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 6892423945.8%

반응 단계

To a solution of 1-methanesulfonyl-5-chloro-spiro[indoline-3,3′-pyrrolidine] (725 mg) in acetonitrile (40 ml) were added diisopropylethylamine (0.66 ml) and 4-chlorocinnamyl chloride (467 mg). The resulting solution was stirred at room temperature for 12 hours, diluted with ethyl acetate, washed with water, brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by silica gel chromatography (eluent cyclohexane:ethyl acetate 6:4) to afford 1-methanesulfonyl-5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (500 mg) which was characterised by its mass and NMR spectra. MS (ES+) 437/439 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08299058B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-88ecd14c632f41698b848a2811aad99c
출처 메모uspto-grants-2012_10