HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-((4-Methylpiperazin-1-yl)methyl)aniline → HCID 66576872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-((4-Methylpiperazin-1-yl)methyl)aniline | HCID 3153996 | — |
| Reactant | HCID 79073638 | HCID 79073638 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 66576872 | HCID 66576872 | 20% |
Reaction Steps
The title compound was prepared according to synthesis procedure B described above from 2-chloro-4-(3-methoxyphenyl)-5-methylpyrimidine and 4-((4-methylpiperazin-1-yl)methyl)aniline in 20% yield (yellow solid) after flash chromatography (CH2Cl2/CH3OH 99:1 gradually increasing to 95:5). 1H NMR (400 MHz, CDCl3): δ 8.29 (s, 1H), 7.59 (d, 2H, J=8.2 Hz), 7.37 (t, 1H, J=8.0 Hz), 7.24 (d, 2H, J: not calculated due to overlapping peaks), 7.16 (m, 2H), 6.98 (d, 1H, J=8.2 Hz), 3.85 (s, 3H), 3.49 (s, 2H), 2.57 (bs, 8H), 2.36 (s, 3H), 2.24 (s, 3H); MS (ESI): 404.4 [M+H]+, 202.9 [M+2H]2+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901120B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-dc9dfd1f0b2d457e998377b9676d9e06 |
| Source note | uspto-grants-2014_12 |