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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488270Generated: November 1, 2026

HCID 131736866, compound → HCID 131736865, compound

https://huagongshe.com/reaction/1488270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131736866HCID 131736866—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
ProductHCID 131736865HCID 131736865—

Reaction Steps

To a solution of benzyl (2-{[2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1→3)-[2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1→6)]-2-O-benzoyl-4-O-benzyl-β-D-glucopyranosyl]oxy}ethyl)carbamate (3.39 g, 1.984 mmol) in CH3OH (30 mL) was added NaOCH3 (0.4 mL, 0.2 mmol, 0.5 M in CH3OH). After stirring at rt for 24 hr, amberlite IR 120 (H) ion exchange resin (pre-washed with CH3OH 3×30 mL) was added to the reaction mixture. The resulting mixture was allowed to stir for additional 15 min. The resin was filtered off and washed with CH3OH (3×5 mL). The filtrate was concentrated to give the title compound. UPLC Method B: calculated for C35H49NO18 771.29, observed m/e: 772.42 [M+1]; Rt=2.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427475B2
Source datasetuspto-grants-2016_08
ORD IDord-d1b82cf3590b4ec68106749117ecce04
Source noteuspto-grants-2016_08