Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 59239359 | HCID 59239359 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59239148 | HCID 59239148 | — |
Reaction Steps
6-benzyl-4-morpholino-2-(4-nitrophenyl)-5H-pyrrolo[3,4-d]pyrimidin-7(6H)-one (cy) (0.112 g, 0.260 mmol), stannous chloride dihydrate (0.310 g, 1.36 mmol) and ethanol (2.00 mL) were combined and stirred at 80° C. for 1 hour. The mixture was diluted with H2O and 10% MeOH in dichloromethane, extracted 3 times with 10% MeOH in dichloromethane. The combined organic extract was dried over Magnesium sulfate and concentrated to give compound cz (0.083 g, 80%): LC-MS: m/z=+434 (M+H)+; 1H NMR (400 MHz, DMSO) δ 9.10 (s, 2H), 7.24 (d, J=8.6, 2H), 7.14 (s, 2H), 6.91 (d, J=8.6, 2H), 4.64 (d, J=27.1, 4H), 3.80-3.60 (m, 11H).
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-e4cfde2a52f74a5baed3cf030a3fe541 |
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| Source note | uspto-grants-2012_04 |
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