HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Fluorophenethyl)piperazin-2-one → tert-Butyl 7-(4-(4-fluorophenethyl)-2-oxopiperazin-1-yl)-3,5-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Fluorophenethyl)piperazin-2-one | HCID 57514761 | — |
| Reactant | tert-Butyl 7-bromo-3,5-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate | HCID 67986822 | — |
| Product | tert-Butyl 7-(4-(4-fluorophenethyl)-2-oxopiperazin-1-yl)-3,5-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate | HCID 67986823 | 58% |
Reaction Steps
tert-Butyl 7-bromo-3,5-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate (enantiomer A) (180 mg, 0.474 mmol) and 4-(4-fluorophenethyl)piperazin-2-one (104 mg, 0.474 mmol) were reacted following the procedure for Example 2 (step f) to provide the title compound (144 mg, 58%) as a yellow solid: ESI MS m/z 521 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697700B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-7f06e2fbf3fd4aee832ccfaf4cf76047 |
| Source note | uspto-grants-2014_04 |