HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131736866, compound → HCID 131736865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131736866 | HCID 131736866 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131736865 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09427475B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d1b82cf3590b4ec68106749117ecce04 |
| Source note | uspto-grants-2016_08 |