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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261734Generated: November 2, 2026

Acetic Acid → HCID 56847104, compound

https://huagongshe.com/reaction/1261734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 66778751HCID 66778751—
ReactantHCID 86662665HCID 86662665—
SolventMethanolHCID 887—
ProductHCID 56847104HCID 5684710436%

Reaction Steps

To a vial containing methyl 6-(benzylcarbamoyl)-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxylate was added MeOH (1 mL) and hydroxylamine potassium salt (1 mL, 1.76 mmol, 1.76 M in MeOH) and the resulting mixture was shaken at rt for 13 h. The solution was quenched with acetic acid (0.200 mL, 3.52 mmol) before being concentrated. To the resulting residue was added DMSO (1.2 mL) and it was purified via prep-HPLC to yield N6-benzyl-N2-hydroxy-7,8-dihydro-1,6-naphthyridine-2,6(5H)-dicarboxamide (0.0113 g, 36.0%). LC-MS: (FA) ES+ 327; 1H NMR (Methanol-d4, 400 MHz) 7.86 (d, J=7.8 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 7.25-7.19 (m, 5H), 4.68 (s, 2H), 4.39 (s, 2H), 3.79 (t, J=6.0 Hz, 2H), 3.03 (t, J=6.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471026B2
Source datasetuspto-grants-2013_06
ORD IDord-0fb38855422a444cacb3505a82379e8d
Source noteuspto-grants-2013_06