HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387668Generated: October 30, 2026
Hydrochloric Acid → HCID 25206608, compound
https://huagongshe.com/reaction/387668
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 25206609 | HCID 25206609 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 25206608 | HCID 25206608 | — |
Reaction Steps
300 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-7-[(methylsulfonyl)amino]-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. 0.4 cm3 of a 4N solution of hydrochloric acid in dioxane is added while stirring at a temperature of 20° C. The reaction mixture precipitates. The solid is washed with three lots of 5 cm3 of isopropyl ether and dried under vacuum at a temperature of 50° C. 280 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-7-[(methylsulfonyl)amino]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxamide hydrochloride (1:1) are obtained in the form of a white powder.
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-dccf01c5a5e048db91b8725cc44bbb83 |
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| Source note | uspto-grants-2013_02 |
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