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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444673Generated: October 30, 2026

Acetic Acid → 1-(cyclobutylamino)-4-hydroxyquinolin-2(1H)-one

https://huagongshe.com/reaction/1444673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclobutanoneHCID 14496—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-amino-4-hydroxyquinolin-2(1H)-oneHCID 59168807—
SolventMethanolHCID 887—
Product1-(cyclobutylamino)-4-hydroxyquinolin-2(1H)-oneHCID 5916880360%

Reaction Steps

A solution of 1-amino-4-hydroxyquinolin-2(1H)-one (0.516 g, 2.9 mmol) and cyclobutanone (1.05 g, 15.0 mmol) in acetic acid (0.90 g, 15.0 mmol) and methanol (20 mL) was treated portion wise with sodium cyanoborohydride (0.94 g, 15.0 mmol), stirred for 48 hours and concentrated. The residue was treated with 0.5 M aqueous sodium bicarbonate, acidified to pH 2 with 1 M hydrochloric acid and extracted with ethyl acetate. The ethyl acetate was washed with brine, dried over sodium sulfate, filtered and concentrated, The crude material was chromatographed on silica gel eluting with 3:2 hexane/ethyl acetate to give 1-(cyclobutylamino)-4-hydroxyquinolin-2(1H)-one (0.400 g, 60%). MS (ESI+) m/z 231 (M+H)+. 1H NMR (300 MHz, DMSO-d6) δ 1.52 (m, 1H) 1.63 (m, 1H) 1.96 (m, 4H) 3.64 (m, 1H) 5.91 (s, 1H) 6.26 (d, J=6.62 Hz, 1H) 7.20 (t, J=8.09 Hz, 1H) 7.61 (m, 1H) 7.84 (m, 2H) 11.42 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662958B2
Source datasetuspto-grants-2010_02
ORD IDord-06f90f41c1ff469cb5089d98e063b423
Source noteuspto-grants-2010_02