HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387655Generated: October 30, 2026
Hydrochloric Acid → HCID 25206448, compound
https://huagongshe.com/reaction/387655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 25206449 | HCID 25206449 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 25206448 | HCID 25206448 | — |
Reaction Steps
330 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-7-[methyl(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. 1 cm3 of a 2M solution of hydrochloric acid in ethyl ether is added, while stirring under argon, at a temperature of 20° C. The reaction mixture precipitates. The solid is filtered, washed with 5 cm3 of ethyl ether and dried under vacuum at a temperature of 35° C. for 3 h. 310 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-7-[methyl(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-d6ea345be7324459ba58f428d2ce8161 |
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| Source note | uspto-grants-2013_02 |
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