HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 9-(4-Methyl-piperazin-1-yl)-4-thia-10a-aza-benzo[f]azulene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | 9,10-Dihydropyrrolo[2,1-b][1,3]benzothiazepin-9-one | HCID 10822568 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-(4-Methyl-piperazin-1-yl)-4-thia-10a-aza-benzo[f]azulene | HCID 9796255 | 84% |
Reaction Steps
A solution of 9,10-dihydropyrrolo[2,1-b][1,3]benzothiazepin-9-one (0.24 g, 1.11 mmol), N-methylpiperazine (0.55 mL, 0.50 g, 4.99 mmol) and trimethylsilyl triflate (0.55 mL, 0.68 g, 3.05 mmol) was heated at 120° C. under stirring, after a few minutes further 0.55 mL of N-methylpiperazine were added and the reaction was kept for 3 hours at 120° C. After that time water was added and was extracted with dichloromethane. The organic layer was dried over sodium sulphate, filtered and evaporated to give the crude product that was purified by means of a flash chromatography (20% methanol in ethyl acetate) to afford 0.114 g of the pure title compound as a yellowish solid (84% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710041B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-839aa6d361804ea2a67fc94a608c6737 |
| Source note | uspto-grants-2004_03 |