HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Methylpiperazin-1-yl)benzene-1,2-diamine → HCID 178494100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Methylpiperazin-1-yl)benzene-1,2-diamine | HCID 21877341 | — |
| Reactant | HCID 59784178 | HCID 59784178 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178494100 | HCID 178494100 | 10.5% |
Reaction Steps
To mixture of 2-hydroxy-5-(2-methoxy-pyridin-3-yl)-benzaldehyde (57 mg, 0.25 mmol) and 3-(4-methyl-piperazin-1-yl)-benzene-1,2-diamine (51 mg, 0.25 mol) was added DMA (1 mL) and the resulting solution was stirred at the room temperature for 15 min, heated at 110° C. for 15 h open to the air, concentrated under reduced pressure. The residual crude was purified by chromatography (500:10:1 CH2Cl2/MeOH/28% aqueous NH4OH) to afford the title compound (10.8 mg, 10.5%). 1H NMR (MeOH-d4) δ 2.41 (s, 3H), 2.78 (m, 4H), 3.49 (m, 4H), 3.97 (s, 3H), 6.72 (m, 1H) 7.05-7.20 (4H), 7.56 (d, J=9 Hz, 1H), 7.78 (d, J=9 Hz, 1H), 8.10-8.13 (2H). ESI-MS m/z 416.5 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629147B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-b1f9923507be4a2289676a93c0497726 |
| Source note | uspto-grants-2014_01 |