HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 7-bromo-2-chloro-4-(piperazin-1-yl)-5H-pyrimido[5,4-b]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 7-bromo-2,4-dichloro-5H-pyrimido[5,4-b]indole | HCID 58118487 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-bromo-2-chloro-4-(piperazin-1-yl)-5H-pyrimido[5,4-b]indole | HCID 58118544 | 87% |
Reaction Steps
1.3 g (4.10 mmol) 7-bromo-2,4-dichloro-5H-pyrimido[5,4-b]indole (Example 4) and 1.3 g (14.8 mmol) piperazine were heated in 50 ml toluene at 65° C. for 3 h. Then, the solvent was removed and the residue was suspended in water and sucked off. 1.3 g (87%) 7-bromo-2-chloro-4-(piperazin-1-yl)-5H-pyrimido[5,4-b]indole was obtained. ESI-MS [m/z]: 366, 368 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664233B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-54d8d0742a374a33b21a6e256fe094b4 |
| Source note | uspto-grants-2014_03 |