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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83987생성일: 2026년 10월 25일

Triethylamine → 1-(2-Chloropyridin-4-yl)carbonyl-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]

https://huagongshe.com/reaction/83987

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물2-Chloropyridine-4-carbonyl chlorideHCID 2800003—
반응물5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 68930649—
용매DichloromethaneHCID 6344—
생성물1-(2-Chloropyridin-4-yl)carbonyl-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 8662736349%

반응 단계

A solution of 5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (150 mg) and triethylamine (0.24 ml) in dichloromethane (5 ml) at 0° C. under argon was treated with 2-chloro-isonicotinoyl chloride (147 mg). The resulting solution was stirred at room temperature for 1 hour, poured into saturated aqueous sodium bicarbonate, extracted with ethyl acetate, dried (Na2SO4) and concentrated in vacuo. Silica gel chromatography of the residue (eluent cyclohexane:ethyl acetate 6:4) afforded the title compound, 1-(2-chloropyridin-4-yl)carbonyl-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (95 mg), which was characterised by its mass and NMR spectra. MS (ES+) 498/500 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846907B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-274243220eae4859921604cb8134f577
출처 메모uspto-grants-2014_09