Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopiperidin-2-one | HCID 118171 | — |
| Reactant | tert-Butyl 4-(6-aminopyrimidin-4-yl)piperazine-1-carboxylate | HCID 21934614 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 21934693 | HCID 21934693 | — |
Reaction Steps
3-Bromopiperidin-2-one 51-1 (0.15 g, 0.87 mmol) was dissolved in n-butanol (4 mL) then triethyl amine (0.26 g, 2.60 mmol) was added followed by tert-butyl piperazine-1-carboxylate 12-1 (0.16 g, 0.87 mmol). This was then stirred at 150° C. for 1.5 hours and then the solid was filtered off, washed with n-butanol and then ethyl ether. Hi-Res MS: calc: 284.1969 found: 284.1966. 1H-NMR (CDCl3): 3.45 (br s, 2H); 3.26 (br s, 2H); 3.13 (complex, 3H); 2.74(m, 1H); 2.62(m, 1H); 1.98(m, 1H); 1.77(m, 1H); 1.55(complex, 3H); 1.45(t, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07115597B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-44e4dce697cd4a18a6ddd654de9ad96a |
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| Source note | uspto-grants-2006_10 |
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