Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Barbituric Acid | HCID 6211 | — |
| Reactant | HCID 131726347 | HCID 131726347 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58847031 | HCID 58847031 | — |
Reaction Steps
2-(cis-2-methyl-6-propylmorpholin-4-yl)-5-nitrobenzaldehyde (446 mg, 1.53 mol) is combined with barbituric acid (217 mg, 1.53 mmol, Aldrich) in a vial with MeOH (6 mL). The sealed reaction is heated to 80° C. on a shaker block for 19 hours and then the solvent is removed by rotary evaporation. The product is purified 2× on a Biotage Flash 75M using 10% MTBE in CH2Cl2 eluent. The product is dried under vacuum at 100° C. yielding a yellow-orange solid. 1H NMR (400 MHz, ACETONITRILE-D3) δ ppm 0.95, 1.00, 1.47, 3.04, 3.34, 3.56, 3.95, 4.14, 6.85, 7.77, 8.02, 9.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420646B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-66cf24cd5088471fa5b17ffc28157701 |
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| Source note | uspto-grants-2013_04 |
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