戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1009813作成日:2026年10月23日

Hydrochloric Acid → Trandolapril

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydrideHCID 4639425—
反応物(2S,3aR,7aS)-Octahydro-1H-indole-2-carboxylic acidHCID 7018901—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物TrandolaprilHCID 548472730.7%

反応手順

(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%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07973173B2
出典データセットuspto-grants-2011_07
ORD IDord-0ee4d9cde17e43c3adf3bdc46d940d6c
出典メモuspto-grants-2011_07