Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 178471769 | HCID 178471769 | — |
| Product | HCID 178471765 | HCID 178471765 | — |
Reaction Steps
A mixture of the product from Example 48A (100 mg, 0.27 mmol) and urea (33 mg, 0.54 mmol) in N,N-dimethylformamide (5 mL) was heated at 90-95° C. under N2 for 2 hours. The mixture was concentrated, and purified on a RP-HPLC to provide the title product. 1H NMR (500 MHz, DMSO-d6) δ ppm 1.13 (m, 2H), 1.19 (t, J=7.05 Hz, 3H), 1.48 (m, 2H), 1.69-1.85 (m, 5H), 2.22 (d, J=6.75 Hz, 2H), 2.47 (m, 1H), 4.07 (q, J=7.05 Hz, 3H), 4.14 (m, 1H), 7.28 (d, J=8.29 Hz, 2H), 7.63 (d, J=8.29 Hz, 2H), 8.29 (s, 1H), 8.95 (br s, 1H), 11.50 (br s, 1H); MS (ESI) m/z 356.9 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202878B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-d136f6616fda4715a4f337299f297e02 |
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| Source note | uspto-grants-2012_06 |
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