Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 5-Chloro-7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidine | HCID 22386546 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22386543 | HCID 22386543 | — |
Reaction Steps
To the suspension of 5-chloro-7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidine (57.94 mg, 0.2 mmol) and 4-aminobenzonitrile (35.44 mg, 0.3 mmol) in the mixture of 2.5 ml 2-propanol and 1.5 ml H2O was added conc.HCl. Then the mixture was stirred at 85 to 90° C. overnight, and cooled to room temperature. The produced solid was collected by filtration and purified by preparative TLC to give the desired product of 4-[7-(3,4-dimethoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-ylamino]-benzonitrile. (38 mg, 51.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06911443B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-83391473ffd5457d9b7d481fe845167a |
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| Source note | uspto-grants-2005_06 |
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