Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 86640112 | HCID 86640112 | — |
| Product | HCID 136079653 | HCID 136079653 | — |
Reaction Steps
Step 3—Synthesis of compound vb: (S)-1-methyl-N-(4-(4-(3-methylmorpholino)-7-(pyrimidin-2-yl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenylcarbamothioyl)hydrazinecarboxamide (0.113 g, 0.000211 mol) and Ethanol (3.7 mL, 0.063 mol) were combined and the reaction was microwaved on 300 watts, 150° C. for 30 minutes on a CEM microwave. The reaction mixture was chromatographed through silica gel (0-5% MeOH in dichloromethane) and purified by HPLC. 1H NMR (400 MHz, DMSO) δ 9.34 (s, 1H), 8.43 (d, J=4.7, 2H), 8.22 (d, J=8.8, 2H), 7.47 (d, J=8.8, 2H), 6.69 (t, J=4.7, 1H), 4.88 (d, J=18.7, 1H), 4.73 (d, J=18.7, 1H), 4.17-4.04 (m, 2H), 3.91-3.79 (m, 2H), 3.70 (dd, J=11.3, 2.6, 1H), 3.61 (dd, J=9.9, 6.5, 3H), 3.43 (d, J=11.3, 1H), 3.23 (s, 3H), 2.73 (s, 2H), 1.25 (d, J=6.6, 3H). LC/MS-m/z+501.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163763B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-252a31549c1d48b6bde148ec498aa0f7 |
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| Source note | uspto-grants-2012_04 |
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