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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776160Generated: November 1, 2026

Dimethylmethylenammonium chloride → 2-Dimethylaminomethyl-9-hydroxy-4H-1,3-thiazolo[5,4-c]isoquinolin-5-one hydrochloride

https://huagongshe.com/reaction/1776160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylmethylenammonium chlorideHCID 11051579—
Reactant9-Hydroxy-4H-1,3-thiazolo[5,4-c]isoquinolin-5-oneHCID 58016060—
Solventacetonitrile N,N-dimethylformamideHCID 21891449—
Product2-Dimethylaminomethyl-9-hydroxy-4H-1,3-thiazolo[5,4-c]isoquinolin-5-one hydrochlorideHCID 6707643113%

Reaction Steps

To a solution of 9-hydroxy-4H-1,3-thiazolo[5,4-c]isoquinolin-5-one in DMF/acetonitrile (3 ml, 1:2) was added dimethyl-methylene-ammonium chloride (0.043 g, 0.46 mmol) and the resulting mixture was refluxed under Ar for 42 hours. After cooling and concentration, the residue was purified via flash chromatography on SiO2 to give the title compound (0.008 g, a 13% yield) as solid. m.p.>250° C.; 1H NMR (400 MHz, DMSO) δ 2.36 (s, 6H, N(CH3)2), 3.93 (m, 2H, CH2N), 7.24 (d, 1H, Ar), 7.44 (t, 1H, Ar), 7.74 (d, 1H, Ar), 10.23 (s, 1H, OH), 12.30 (s, 1H, NH); 13C NMR (100.6 MHz, DMSO) δ 46.83, 61.38, 119.94, 120.56, 121.00, 126.83, 129.95, 131.75, 137.39, 154.41, 162.54.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265769B2
Source datasetuspto-grants-2016_02
ORD IDord-8bade023557c4cb8836ecb87955760a5
Source noteuspto-grants-2016_02