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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552105Generated: October 27, 2026

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

https://huagongshe.com/reaction/552105

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 1M 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, 1 H) 1.63 (m, 1 H) 1.96 (m, 4 H) 3.64 (m, 1 H) 5.91 (s, 1 H) 6.26 (d, J=6.62 Hz, 1 H) 7.20 (t, J=8.09 Hz, 1 H) 7.61 (m, 1 H) 7.84 (m, 2 H) 11.42 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951800B2
Source datasetuspto-grants-2011_05
ORD IDord-272514cdc9ac4e1e9cfa0075424d1245
Source noteuspto-grants-2011_05