HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105212Generated: October 31, 2026
1-Methylpiperazine → HCID 11386498, compound
https://huagongshe.com/reaction/2105212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 86610854 | HCID 86610854 | — |
| Product | HCID 11386498 | HCID 11386498 | 72.5% |
Reaction Steps
A mixture of 6-[(4-methylphenylsulphonyloxy)methyl]-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl}-4-(5-methyl-2-N-[4-methylphenylsulphonyl]-1H-pyrazol-3-ylamino)pyrimidine (Method 52) (214 mg, 0.295 mmol) and 1-methylpiperazine (3.0 ml, 27.1 mmol) was heated at reflux for 4 hours. The volatiles were removed by evaporation and the residue purified by reverse phase HPLC using a C18 column eluting with water/acetonitrile/TFA (95:5:0.2 decreasing in polarity to 0:100:0.2). Product containing fractions were combined and passed through a 50 g isolute SCX-2 ion exchange column. The column was eluted with methanol to elute any neutrals, followed by 7M methanolic ammonia to elute the product. The solvent was removed by evaporation of give the title compound (107 mg, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07579349B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-168fcc27fde9451bbcd4c7ed5e0b3cec |
|---|
| Source note | uspto-grants-2009_08 |
|---|