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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amine | HCID 71743379 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-yl)propionamide | HCID 86685953 | 92.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133158B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-07d4dbf302264553bbb2ccd3b0197313 |
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| Source note | uspto-grants-2015_09 |
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