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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261736Generated: November 2, 2026

Acetic Acid → HCID 56847160, compound

https://huagongshe.com/reaction/1261736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 66778571HCID 66778571—
ReactantHCID 86662665HCID 86662665—
SolventMethanolHCID 887—
ProductHCID 56847160HCID 5684716028.3%

Reaction Steps

To a microwave vial containing methyl 6-(butylsulfonyl)-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). The solution was shaken at rt for 1 h, then acetic acid (0.102 mL, 1.8 mmol) was added to quench excess base. The solvent was then concentrated. To the resulting residue was added DMSO (1.2 mL) and after filtration, the solution underwent purification via prep-HPLC to give 6-(butylsulfonyl)-N-hydroxy-5,6,7,8-tetrahydro-1,6-naphthyridine-2-carboxamide (13.3 mg, 28.3%). LC-MS: (FA) ES+ 314; 1H NMR (Methanol-d4, 300 MHz) δ 7.97 (d, J=8.1 Hz, 1H), 7.76 (d, J=7.9 Hz, 1 H), 4.59 (s, 2H), 3.70 (t, J=6.0 Hz, 2H), 3.13 (m, 4H), 1.77 (m, 2H), 1.47 (m, 2H), 0.95 (t, J=7.3 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471026B2
Source datasetuspto-grants-2013_06
ORD IDord-416a12599f764655b1a209bab4370858
Source noteuspto-grants-2013_06