HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397291Generated: October 29, 2026
HCID 69624759, compound → HCID 69624726, compound
https://huagongshe.com/reaction/397291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69624759 | HCID 69624759 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69624726 | HCID 69624726 | 62.4% |
Reaction Steps
To a solution of (2R*)-2-[N-(carbobenzyloxy)amino]-3-[2-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)indole-3-yl]propionic acid [compound (XII-1) wherein R1 to R4 are benzyl and Ar is phenyl](181 mg (0.210 mmol)) in ethanol (45 ml) was added 20% palladium hydroxide-carbon catalyst (150 mg) and the mixture was stirred at about 60° C. for about 11 hours under atmospheric pressure in the presence of hydrogen. The reacted solution was filtrated on Celite and the filtrate was concentrated. The residue was fractionated by high performance liquid chromatography [column: YMC-Pack ODS-AM SH-365-10AM, 500×30 mm, S-10, 120 Å; temperature: room temperature; migrating layer: 5% acetonitrile-water; flow rate: 40 ml/min.; detection: 278 nm (UV)] and then freeze-dried to give 48 mg (yield 62%) of (2R*)-2-amino-3-[2-(α-mannopyranosyl)indole-3-yl]propionic acid [compound (XIII-1)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610502B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-c9735d2eb32c498cbc12c6cdbe5a2751 |
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| Source note | uspto-grants-2003_08 |
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