Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86641916 | HCID 86641916 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67410437 | HCID 67410437 | — |
Reaction Steps
(R)-tert-Butyl 2-(4-(oxazol-5-yl)phenylamino)-4-((tetrahydrofuran-2-yl)methylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (323 mg, 0.66 mmol) was dissolved in methanol (3 mL). Hydrochloric acid (0.020 mL, 0.66 mmol) was added and the reaction mixture was stirred at 80° C. for 1 h. The solvent was evaporated under reduced pressure and the crude was used as such in the subsequent step. MS (ES+) m/z 393.3 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188101B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c16e750a3d704a81823a8c1629b901c3 |
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| Source note | uspto-grants-2012_05 |
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