HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399153Generated: October 31, 2026
HCID 21333283, compound → HCID 21333254, compound
https://huagongshe.com/reaction/2399153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21333283 | HCID 21333283 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21333254 | HCID 21333254 | — |
Reaction Steps
A solution of 11.7 g of 1-{N-benzyl-N-[2-(3-carbamoyl-2-pyridyloxy)-ethyl]-amino}-3-(2-methyl-phenyloxy)-2-propanol in 120 ml of ethanol is hydrogenated in the presence of 1.2 g of a 5% strength palladium-on-charcoal catalyst at 20°-30° C. and under atmospheric pressure until the uptake of hydrogen ceases. The reaction product is worked up analogously to the process described in Example 1, giving crude 1-[2-(3-carbamoyl-2-pyridyloxy)-ethylamino]-3-(2-methyl-phenyloxy)-2-propanol. A solution of 1.5 g of fumaric acid in isopropanol is added thereto and the neutral fumaric acid salt of 1-[2-(3-carbamoyl-2-pyridyloxy)-ethyl-amino]-3-(2-methyl-phenyloxy)-2-propanol thus obtainable, is recrystallised from a mixture of isopropanol and water; melting point 156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04027027 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-04b560eeb509449bb67988bcd442e9fa |
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| Source note | uspto-grants-1977_05 |
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