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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1009812생성일: 2026년 10월 26일

Pyridine → N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride

https://huagongshe.com/reaction/1009812

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물TriphosgeneHCID 94429—
반응물N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanineHCID 5702571—
반응물Disodium dihydrogen phosphate dihydrateHCID 131728993—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydrideHCID 4639425—

반응 단계

Disodium dihydrogen phosphate dihydrate (177 gms; 0.994 moles) was dissolved in water (300 ml) at 35° C. and cooled to ambient temperature. Dichloromethane (250 ml) was charged and stirred for 15 mins. N-[1-(S)-ethoxy carbonyl-3-phenyl propyl]-L-alanine (106 gms; 0.381 moles) was added to the above solution and the reaction mass was cooled to 15° C. Solution of triphosgene (52.8 gms; 0.177 moles) dissolved dichloromethane (40 ml) was added dropwise to the reaction mass in 40 mins at 15-20° C. The reaction mass was further stirred for 30 min. Pyridine (0.5 ml; 0.006 moles) was added and the reaction mass was stirred for 1 hr at 15-20° C. The reaction mass was settled and layers were separated. Organic layer was washed with 2N HCl till the neutral pH obtained. The organic layer was further washed with water and dried over sodium sulphate. The solvent was evaporated to residue (110 gms).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973173B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-f600f994792b486984d622730424ab60
출처 메모uspto-grants-2011_07