Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 86670149 | HCID 86670149 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86670151 | HCID 86670151 | — |
Reaction Steps
To a 20 mL round-bottomed flask charged with 2-((2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)-4-methylbenzonitrile (PREPARATION x83, 52 mg, 0.146 mmol) was added sulfuric acid (1.6 mL, 29.2 mmol). The resulting yellow solution was stirred overnight at room temperature and was subsequently diluted with EtOAc and washed with saturated NaHCO3 to adjust the pH to ˜8. The combined organic layers were dried over MgSO4, filtered, and concentrated to give an orange solid, which was used without further purification. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.88-3.02 (m, 5 H), 3.09-3.18 (m, 3 H), 3.19-3.28 (m, 2 H), 3.41-3.51 (m, 3 H), 3.59-3.71 (m, 2 H), 3.80-3.91 (m, 3 H), 3.91-4.00 (m, 2 H), 4.19-4.29 (m, 3 H), 4.30-4.58 (m, 2 H), 7.16-7.29 (m, 10 H), 7.37-7.45 (m, 2 H), 7.73-7.82 (m, 2 H); ESI-MS m/z [M+H]+ calc'd for C18H20ClN5O2, 374.1; found 374.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045496B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-2cc35bd8f87848749a0e3489725ab6b4 |
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| Source note | uspto-grants-2015_06 |
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