HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661085Generated: October 30, 2026
Hydrochloric Acid → N-[(1S,2R)-1-benzyl-2-hydroxy-3-{[3-(trifluoromethyl)benzyl]amino}propyl]-1-oxo-2-(1-propylbutyl)-1,2-dihydroisoquinoline-5-carboxamide hydrochloride
https://huagongshe.com/reaction/1661085
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-[(1S,2R)-1-benzyl-2-hydroxy-3-{[3-(trifluoromethyl)benzyl]-amino}propyl]-1-oxo-2-(1-propylbutyl)-1,2-dihydroisoquinoline-5-carboxamide | HCID 25204518 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[(1S,2R)-1-benzyl-2-hydroxy-3-{[3-(trifluoromethyl)benzyl]amino}propyl]-1-oxo-2-(1-propylbutyl)-1,2-dihydroisoquinoline-5-carboxamide hydrochloride | HCID 67429965 | — |
Reaction Steps
84 mg of N-[(1S,2R)-1-benzyl-2-hydroxy-3-{[3-(trifluoromethyl)benzyl]-amino}propyl]-1-oxo-2-(1-propylbutyl)-1,2-dihydroisoquinoline-5-carboxamide are dissolved in 4 cm3 of ethyl ether at a temperature close to 20° C. 0.2 cm3 of a 4M solution of hydrochloric acid in dioxane is added while stirring and under argon. The reaction mixture precipitates. The stirring is stopped. The supernatant is removed and 5 cm3 of ethyl ether are added. This operation is carried out three times. The last suspension is concentrated under reduced pressure (5 kPa). 87 mg of N-[(1S,2R)-1-benzyl-2-hydroxy-3-{[3-(trifluoromethyl)benzyl]amino}propyl]-1-oxo-2-(1-propylbutyl)-1,2-dihydroisoquinoline-5-carboxamide hydrochloride (1:1) are obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030320B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-e57830f8a2ee4b49b8ce8b3dfe0ab92a |
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| Source note | uspto-grants-2011_10 |
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