HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 21254910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21255057 | HCID 21255057 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21254910 | HCID 21254910 | 86.8% |
Reaction Steps
0.1 g (1 mmol) of 1-methyl-piperazine in 3 ml of CH2Cl2 was added to a solution of 0.37 g (1 mmol) of 3-benzenesulphonyl-5,7-dichloro-2-methylsulphanyl-pyrazolo[1,5-a]-pyrimidine in 20 ml of CH2Cl2 and stirred at RT for 1 hr. The mixture was poured on to ice-water, adjusted to pH8 with NaHCO3 solution and extracted three times with 30 ml of CH2Cl2. The combined organic phases were dried (MgSO4), filtered and evaporated. Subsequent chromatography (silica gel, CH2Cl2/MeOH 4:1) yielded 0.38 g (86%) of 3-benzenesulphonyl-5-chloro-7-(4-methyl-piperazin-1-yl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine as colorless crystals, m.p.>230°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194410B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-db82d2ad635a4d94bc75eb72c9c68558 |
| Source note | uspto-grants-2001_02 |