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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007165Generated: October 28, 2026

Hydrochloric Acid → Urea, N-[2-[6,7-dihydro-9,10-dimethoxy-4-oxo-2-[(2,4,6-trimethylphenyl)imino]-2H-pyrimido[6,1-a]isoquinolin-3(4H)-yl]ethyl]-

https://huagongshe.com/reaction/1007165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium CyanateHCID 517096—
Reactant4H-?Pyrimido[6,?1-?a]?isoquinolin-?4-?one, 3-?(2-?aminoethyl)?-?2,?3,?6,?7-?tetrahydro-?9,?10-?dimethoxy-?2-?[(2,?4,?6-?trimethylphenyl)?imino]?-HCID 21958492—
SolventWaterHCID 962—
ProductUrea, N-[2-[6,7-dihydro-9,10-dimethoxy-4-oxo-2-[(2,4,6-trimethylphenyl)imino]-2H-pyrimido[6,1-a]isoquinolin-3(4H)-yl]ethyl]-HCID 9934746—

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium cyanate (6.0 g, 0.092 mol) in water (100 ml) was added dropwise to a stirred solution of 9,10-Dimethoxy-2-(2,4,6-trimethylphenylimino)-3-(2-aminoethyl)-3,4,6,7-tetrahydro-2H-pyrimido[6,1-a]isoquinolin-4-one, prepared according to Preparation 4 above (20.0 g, 0.046 mol) in water (600 ml) and 1N HCl (92 ml) at 80° C. After stirring for 2 h at 80° C. the mixture was cooled in an ice-bath and basified with 2N NaOH. The mixture was extracted with dichloromethane (3×200 ml) and the combined extract was dried (MgSO4) and evaporated in vacuo. The resulting yellow foam was purified by column chromatography on silica gel eluting with CH2Cl/MeOH (97:3) and triturated with ether to obtain the title compound as a yellow solid, 11.9 g, 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794391B2
Source datasetuspto-grants-2004_09
ORD IDord-86ba8e28636043e8ae54571ff6bfaa3d
Source noteuspto-grants-2004_09