HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-((4-Methylpiperazin-1-yl)methyl)aniline → HCID 70683482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-((4-Methylpiperazin-1-yl)methyl)aniline | HCID 3153996 | — |
| Reactant | HCID 86673367 | HCID 86673367 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 70683482 | HCID 70683482 | 73% |
Reaction Steps
The title compound was prepared according to synthesis procedure B described above from (2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)(pyrrolidin-1-yl)methanone and 4-((4-methylpiperazin-1-yl)methyl)aniline in 73% yield (yellow solid) after flash chromatography (CH2Cl2/CH3OH 99:1 gradually increasing to 95:5). 1H NMR (400 MHz, CDCl3): δ 9.68 (s, 1H), 8.40 (d, 1H, J=8.2 Hz), 8.04 (s, 1H), 7.46 (d, 2H, J=8.2 Hz), 7.39-7.34 (m, 2H), 7.21 (d, 2H, J=8.2 Hz), 7.06 (t, 1H, J=7.5 Hz), 3.65 (t, 2H, J=7.0 Hz), 3.48 (t, 2H, J=6.3 Hz), 3.44 (s, 2H), 2.44 (bs, 8H), 2.26 (s, 3H), 1.95 (m, 2H), 1.83 (m, 2H); MS (ESI): 506.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901120B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-6b5dffe7dbc64016980dee2aeed4f9b0 |
| Source note | uspto-grants-2014_12 |