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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 4H-?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 | — |
| Solvent | Water | HCID 962 | — |
| Product | 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]- | HCID 9934746 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794391B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-86ba8e28636043e8ae54571ff6bfaa3d |
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| Source note | uspto-grants-2004_09 |
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