Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 59333754 | HCID 59333754 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 46200197 | HCID 46200197 | 47.7% |
Reaction Steps
Hydrogen chloride (2 mL, 0.20 mmol, 2M aq) was added to a solution of tert-butyl 4-(benzylamino)-2-(4-(oxazol-5-yl)phenylamino)-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate (0.1 g, 0.20 mmol, Example 5a) in MeOH (5 mL) and heated in an open reaction vessel to 76° C. for 1 h. The residual solvent was removed under reduced pressure, the crude product was redissolved in DMSO and purified by preparative HPLC to give N4-benzyl-N2-(4-(oxazol-5-yl)phenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine-2,4-diamine (38 mg, 47.5%). MS (ESI+)/(ESI−) m/z 399/397
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-bb392d0e0f6e41b994098021e3563c63 |
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| Source note | uspto-grants-2012_05 |
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