HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylpiperazine → 3-Methyl-1-[(5-nitro-1-benzofuran-7-yl)methyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylpiperazine | HCID 66057 | — |
| Reactant | 7-(Bromomethyl)-5-nitrobenzofuran | HCID 53402971 | — |
| Product | 3-Methyl-1-[(5-nitro-1-benzofuran-7-yl)methyl]piperazine | HCID 66893210 | 95% |
Reaction Steps
The title compound was prepared according to the procedure of Example 112, Step 1, starting from 7-(bromomethyl)-5-nitro-1-benzofuran (120 mg, 70 mol %, 0.39 mmol; Intermediate 64) and 2-methylpiperazine (196 mg, 1.95 mmol). The crude product was purified by flash chromatography (eluent: 4% MeOH, 1% NEt3 in DCM). The title compound (102 mg, 87%) was obtained as a light yellow sticky oil. HPLC 99%, RT=1.60 min (System A; 5-60% MeCN over 3 min), 100%, RT=1.40 min (System B; 5-60% MeCN over 3 min). MS (ESI+) for C14H17N3O3 m/z 276 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820675B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-94bfdf0ab8264c828fd51f5012a15411 |
| Source note | uspto-grants-2010_10 |