Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 10706995 | HCID 10706995 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10732632 | HCID 10732632 | 85% |
Reaction Steps
To the product from Example 13, Step 1 (0.30 g, 1.12 mmol) in ethanol (8 mL) was added tert-butylamine (0.35 mL, 3.36 mmol) and the resulting mixture was heated at 60° C. overnight. The mixture was concentrated, and the residue was dissolved in ethylacetate. Addition of hexanes induced precipitation of product which was filtered and triturated with diethylether/hexanes. Filtration and drying afforded 0.28 g (85%) of the title compound as a yellow solid, three -quarter hydrate: mp 257°-260° C.; 1H NMR (DMSO-d6) d 10.00 (br d, 1H), 8.9 (d, 1H), 8.4 (m, 1H), 8.02 (d, 1H), 7.96 (br d, 1H), 7.86 (dd, 1H), 7.66-7.54 (m, 2H), 1.45 (s, 9H). IR (KBr) 3400, 3200, 2980, 1785, 1680cm-1 ; MS (m/z) 296 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403854 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-e6a3c52e55724f2691baaf1f14ae59f2 |
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| Source note | uspto-grants-1995_04 |
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