HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454556Generated: October 30, 2026
HCID 66990480, compound → HCID 136198173, compound
https://huagongshe.com/reaction/454556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66990480 | HCID 66990480 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136198173 | HCID 136198173 | — |
Reaction Steps
To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-5-(pyridin-4-yl)benzamido)-4-(2-methoxyphenyl)benzoate (0.094 g) in ethyl acetate (2.5 mL) and methanol (3.5 mL), 10% palladium-carbon (19 mg) was added, followed by stirring under a hydrogen atmosphere at room temperature for 3 hours. To the reaction mixture, 10% palladium-carbon (19 mg) was added, followed by stirring under a hydrogen atmosphere at room temperature for 3 hours. The insoluble substance was removed by filtration, and the residue was washed with ethyl acetate and tetrahydrofuran. The filtrate and the washing liquid were combined, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), PSQ100B(spherical), eluent: 65-45% hexane/ethyl acetate] to obtain tert-butyl 2-(2-hydroxy-5-(pyridin-4-yl)benzamido)-4-(2-methoxyphenyl)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-c13c1008347c49af99045e5dba857021 |
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| Source note | uspto-grants-2013_07 |
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