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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908304Generated: October 27, 2026

[(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester → [(3,5-Dihydroxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/1908304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl esterHCID 59513083—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product[(3,5-Dihydroxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl esterHCID 5951307966%

Reaction Steps

A solution of [(3,5-bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester, 26, (3.04 g, 6.79 mmol) in EtOH (100 mL) containing 10% Pd/C (0.300 g) is stirred under an atmosphere of H2 for 22 hours. The suspension is then filtered through Celite™, concentrated under reduced pressure, and the crude product purified over silica (2.5% MeOH/CH2Cl2) to afford 1.20 g (66% yield) of the desired compound as a colorless oil. 1H NMR (250 MHz, CDCl3) δ ppm 11.90 (1H, br s), 8.94 (1H, br s), 8.20 (1H, t, J=5.6 Hz), 7.76 (1H, d, J=2.4 Hz), 6.77 (1H, d, J=2.1 Hz), 4.13 (2H, d, J=5.5 Hz), 1.53 (9H, s). HPLC-MS: m/z 269 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598210B2
Source datasetuspto-grants-2013_12
ORD IDord-c978f7eabbba4e0b905c1c0f468ed51c
Source noteuspto-grants-2013_12