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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402560Generated: October 31, 2026

N5-(1,3-benzodioxol-5-ylmethyl)-N2,3-dibenzyloxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamide → N5-(benzo[d][1,3]dioxol-5-ylmethyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamide

https://huagongshe.com/reaction/402560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN5-(1,3-benzodioxol-5-ylmethyl)-N2,3-dibenzyloxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamideHCID 71589574—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN5-(benzo[d][1,3]dioxol-5-ylmethyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamideHCID 4454102390%

Reaction Steps

The final product of Example 3 above (0.170 g, 0.330 mmol, 1 eq) and 10% Pd/C (5 mg) catalyst were mixed in methanol (4.0 mL) under an atmosphere of hydrogen 1 hour. The catalyst was filtered and reaction mixture was concentrated under vacuum yielding 0.029 g of N5-(benzo[d][1,3]dioxol-5-ylmethyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamide (90% yield) as a white solid; 1H-NMR (400 MHz, MeOD): δ=8.176 (s, 1H), 6.93 (m, 3H), 5.95 (s, 2H), 4.77 (s, 2H), 4.50 (s, 2H); MS-ESI m/z 362 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742123B2
Source datasetuspto-grants-2014_06
ORD IDord-328c033da351429b8b9cf18072b62dbc
Source noteuspto-grants-2014_06