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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1009813생성일: 2026년 10월 23일

Hydrochloric Acid → Trandolapril

https://huagongshe.com/ko/reaction/1009813

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydrideHCID 4639425—
반응물(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acidHCID 7018901—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물TrandolaprilHCID 548472730.7%

반응 단계

(2S,3aR,7aS) octahydro-1H-indole-2-carboxylic acid (65 gms 0.384 moles) was stirred in dichloromethane (200 ml), triethyl amine (30 ml) was added under stirring at ambient temperature for 30 mins. N-[1-(S)-ethoxy carbonyl-3-phenyl propyl]-L-alanine N-carboxy anhydride (110 gms; 0.378 moles) (residue from Step A) dissolved in dichloromethane (50 ml) was added dropwise to the reaction mass at ambient temperature and further stirred for 3 hrs. Water (500 ml) was added and the reaction mass was cooled to 15° C., pH of the reaction mass was adjusted to 4.2 using 2N HCl. The organic layer was separated and aqueous layer reextracted with dichloromethane. The combined organic layer was dried with sodium sulphate and concentrated to residue. The residue was dissolved in ethylacetate at reflux temperature. The reaction mass was cooled to ambient temperature. The resulting solid was filtered and dried under vacuum to get 50 gms of Trandolapril (HPLC purity 99.5%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973173B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-0ee4d9cde17e43c3adf3bdc46d940d6c
출처 메모uspto-grants-2011_07