HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl 4-(1,1-dioxidothietan-3-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-1lambda6-thietane-1,1-dione | HCID 265636 | — |
| Reactant | tert-Butyl 4-(6-aminopyrimidin-4-yl)piperazine-1-carboxylate | HCID 21934614 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Tert-butyl 4-(1,1-dioxidothietan-3-yl)piperazine-1-carboxylate | HCID 21060000 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
3-Chlorothietane 1,1-dioxide 50-1 (0.50 g, 3.56 mmol) was dissolved in n-butanol (4 mL) then triethylamine (1.08 g, 10.67 mmol) was added followed by tert-butyl piperazine-1-carboxylate 12-1 (0.66 g, 3.56 mmol). This was then stirred at 150° C. for 5 hours. Upon cooling the solid was filtered off, washed with n-butanol, ethyl ether and then purified on a silica column to afford 50-2. 1H-NMR (CDCl3): 4.10(complex, 4H); 3.46(t, 4H); 3.19(m, 1H); 2.36(t, 4H); 1.46(s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115597B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-f82d0040d320477bad82445d9a6cd128 |
| Source note | uspto-grants-2006_10 |