HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64829Generated: October 27, 2026
HCID 178427478, compound → HCID 178427477, compound
https://huagongshe.com/reaction/64829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178427478 | HCID 178427478 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178427477 | HCID 178427477 | — |
Reaction Steps
In 150 ml of methanol was dissolved 13.5 g of compound (49) and the compound was catalytically reduced for 5 hours in the presence of 10% palladium-carbon. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue thus formed was dissolved in ethyl acetate and extracted thrice each time with an aqueous sodium hydrogen carbonate solution. The extracts were combined with each other and washed once with ethyl acetate. After acidifying the aqueous layer with 1N hydrochloric acid, the desired compound was extracted with ethyl acetate. Thus, 2.0 g of Nα -t-butyloxycarbonyl-Nim -tosyl-L-histidyl-L-proline (50) was obtained as a foamy product. Also, from the organic layer formed after extracting the product with an aqueous sodium hydrogencarbonate solution, 9.1 g of the starting material (49) was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04610821 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-312530c2073a424489e6d30ff26f99aa |
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| Source note | uspto-grants-1986_09 |
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