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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258556Generated: October 31, 2026

HCID 10757002, compound → HCID 10398374, compound

https://huagongshe.com/reaction/2258556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10757002HCID 10757002—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 10398374HCID 1039837446.4%

Reaction Steps

3-Benzyloxy-4-chloro-5,6-dimethylanthranilic acid (10 mg, 0.03 mmol) was dissolved in EtOH (1.5 mL) and 10% Pd/C (2 mg) was added. Hydrogenation at room temperature and atmospheric pressure for 5 h, filtration, evaporation yielded 7 mg of crude product. Purification by preparative HPLC (Lichrosorb-C18, MeOH-Phosphate buffer (pH3) 50:50) adjusting the pH to 5 with NaHCO3 (aq), concentrating by a stream of N2, extracting with EtOAc (3×5 mL), washing the organic phase with brine, drying (MgSO4) and evaporating afforded the title compound (3 mg). 1H NMR (DMSO-d6): δ 3.3 (br, OH), 3.16 (s, 2 H), 2.16 (s, 3 H), 2.15 (s, 3 H); 13C NMR (DMSO-d6): δ 169.92, 137.87, 135.16, 126.38, 123.51, 121.39, 117.31, 17.72, 15.95; MS (EI, 70 eV): m/z (rel.int.) 217/215 (M+, 21/63),199/197 (20/59), 171/169 (37/100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661183
Source datasetuspto-grants-1997_08
ORD IDord-25341416ff7a40c295419423524f8ddd
Source noteuspto-grants-1997_08