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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277656Generated: October 29, 2026

Propionic Acid → N-(4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-yl)propionamide

https://huagongshe.com/reaction/2277656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amineHCID 71743379—
SolventDichloromethaneHCID 6344—
ProductN-(4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-yl)propionamideHCID 8668595392.1%

Reaction Steps

To a stirred brown solution of 4-bromo-5,6,7,8-tetrahydroisoquinolin-8-amine (318 mg, 1.4 mmol) and propionic acid (114 mg, 1.54 mmol) in CH2Cl2 (7.0 mL) at 0° C. under argon was added EDCI (63.3 mg, 0.330 mmol). Stirring was continued overnight and the reaction mixture was allowed to warm up to room temperature. The reaction mixture was poured onto aq. 10% KH2PO4 solution followed by extraction with AcOEt (3×). The organic phases were washed once with aq. 10% KH2PO4, aq. sat. NaHCO3 and with aq. sat. NaCl solution; the combined organic phases were dried over Na2SO4, filtered and evaporated. The residue was dissolved in CH2Cl2, evaporated with n-pentane (3×) to ca. 10 ml each time, while the product precipitated; then, the solvent was decanted and the residue washed twice with n-pentane to afford the title compound (0.365 g, 92%) as light brown solid. MS: 283.0 (M+H+, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133158B2
Source datasetuspto-grants-2015_09
ORD IDord-07d4dbf302264553bbb2ccd3b0197313
Source noteuspto-grants-2015_09