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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402569Generated: October 31, 2026

N2,3-bis(benzyloxy)-N5-(3,4-dichlorobenzyl)-4-(hydroxymethyl)pyridine-2,5-dicarboxamide → N5-(3,4-dichlorobenzyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamide

https://huagongshe.com/reaction/402569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2,3-bis(benzyloxy)-N5-(3,4-dichlorobenzyl)-4-(hydroxymethyl)pyridine-2,5-dicarboxamideHCID 44539697—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN5-(3,4-dichlorobenzyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamideHCID 445411154.7%

Reaction Steps

Product 15 of example 15 (0.03 g, 0.330 mmol,) and 10% Pd/C (25 mg) catalyst were stirred in methanol (4.0 mL) under an atmosphere of hydrogen for 1 hour. The catalyst was filtered and the reaction mixture was concentrated under vacuum to give 0.006 g of N5-(3,4-dichlorobenzyl)-N2,3-dihydroxy-4-(hydroxymethyl)pyridine-2,5-dicarboxamide as a white solid; 1H-NMR (400 MHz, dmso): δ=13.01 (s, 1H), 12.0 (s, 1H), 9.51 (s 1H), 9.02 (t 1H), 8.11 (s, 1H), 7.60 (d 1H), 7.40 (m, 2H), 4.68 (s, 2H), 4.48 (s, 2H); MS-ESI m/z 386 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742123B2
Source datasetuspto-grants-2014_06
ORD IDord-1edc056295b243aabfe2efaf88023a45
Source noteuspto-grants-2014_06