HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273870Generated: November 1, 2026
Hydrochloric Acid → HCID 53728481, compound
https://huagongshe.com/reaction/273870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 53713896 | HCID 53713896 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53728481 | HCID 53728481 | 94.1% |
Reaction Steps
To a solution of (R)-(-)-1-(4-benzyloxybutyl)-5-[2-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indoline-7-carboxamide (200 mg) in ethanol (3.3 ml) were added a 1N hydrochloric acid (0.8 ml) and 10% palladium on carbon (20 mg), and the mixture was stirred at room temperature for 4 hours under an atmosphere of hydrogen. After the catalyst was filtered off, the filtrate was concentrated under reduced pressure. To the concentrate were added water (12 ml) and sodium carbonate (106 mg), and the mixture was stirred for overnight at room temperature. The precipitated crystals were collected, washed with water, and dried at 50° C. under reduced pressure to give 160 mg of (R)-(-)-1-(4-hydroxybutyl)-5-[2-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indoline-7-carboxamide melting at 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387603 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-ee0e401d09b943509ec5779e212e075b |
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| Source note | uspto-grants-1995_02 |
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