HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387627Generated: October 30, 2026
Hydrochloric Acid → N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxamide hydrochloride
https://huagongshe.com/reaction/387627
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 25206289 | HCID 25206289 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxamide hydrochloride | HCID 25206288 | — |
Reaction Steps
40 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxamide are dissolved in 10 cm3 of ethyl ether at a temperature close to 20° C. 3 cm3 of a 1M hydrochloric acid solution in ether are added while stirring under argon. The reaction mixture precipitates. The precipitate is filtered through sintered glass, washed with 3 lots of 5 cm3 of ethyl ether then dried in a desiccator under vacuum at 35° C. for 2 h. 129 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-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 | US08372864B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-bff53b1f390540749d0896dc2a466744 |
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| Source note | uspto-grants-2013_02 |
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