Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 12004072 | HCID 12004072 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59021464 | HCID 59021464 | 55% |
Reaction Steps
A mixture of 1-(7-(7-(3-chloropyridin-2-yl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-ylamino)-3,4-dihydro-4,4-dimethylisoquinolin-2(1H)-yl)ethanone (10 mg), acetonitrile (2 mL), and 5 N HCl (0.5 mL) was heated overnight at 90° C. The cooled solution was treated with aq. Na2CO3, extracted with EtOAc (15 mL×3). The combined organic layers were washed with brine, dried, and evaporated. The residue was purified by TLC to give a light yellow solid (5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414131B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-6754487290c146d8bf298749b0b459ef |
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| Source note | uspto-grants-2008_08 |
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