HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213713Generated: October 29, 2026
Sodium Cyanate → 3-(N-Carbamoyl-4-aminobutyl)-9,10-dimethoxy-2-(2,4,6-trimethylphenylimino)-3,4,6,7-tetrahydro-2H-pyrimido[6,1-a]isoquinolin-4-one
https://huagongshe.com/reaction/2213713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 3-(4-Aminobutyl)9,10-dimethoxy-2-(2,4,6-trimethylphenylimino)-3,4,6,7-tetrahydro-2H-pyrimido[6,1-a]isoquinolin-4-one | HCID 21958496 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(N-Carbamoyl-4-aminobutyl)-9,10-dimethoxy-2-(2,4,6-trimethylphenylimino)-3,4,6,7-tetrahydro-2H-pyrimido[6,1-a]isoquinolin-4-one | HCID 9935956 | 64.1% |
Reaction Steps
Sodium cyanate (0.28 g, 4.32 mmol) in water (6 ml) was added dropwise to a stirred solution of 2 (1.0 g, 2.16 mmol) in water (30 ml) and 1N HCl (4.3 ml) at 80° C. After 2 h at 80° C. the mixture was cooled and extracted with dichloromethane (3×20 ml) and the extract dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography on silica gel [dichloromethane/methanol (97:3)] to obtain the title compound (0.70 g, 64%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105663B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-1a3cef5bde104658b2cc46f36e7a84b7 |
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| Source note | uspto-grants-2006_09 |
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