Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009813Generated: October 24, 2026

Hydrochloric Acid → Trandolapril

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantN-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydrideHCID 4639425—
Reactant(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acidHCID 7018901—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTrandolaprilHCID 548472730.7%

Reaction Steps

(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%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973173B2
Source datasetuspto-grants-2011_07
ORD IDord-0ee4d9cde17e43c3adf3bdc46d940d6c
Source noteuspto-grants-2011_07