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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397291Generated: October 29, 2026

HCID 69624759, compound → HCID 69624726, compound

https://huagongshe.com/reaction/397291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69624759HCID 69624759—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178502593HCID 178502593—
SolventEthanolHCID 702—
ProductHCID 69624726HCID 6962472662.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610502B1
Source datasetuspto-grants-2003_08
ORD IDord-c9735d2eb32c498cbc12c6cdbe5a2751
Source noteuspto-grants-2003_08