HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → HCID 12018685, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(4-Amino-phenyl)-2-p-tolyl-2H-pyrazol-3-ylamine | HCID 786192 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12018685 | HCID 12018685 | — |
Reaction Steps
To a solution of 1-(4-tolyl)-3-(4-aminophenyl)-5-aminopyrazole (0.1 g, 0.4 mmol) in CH2Cl2 (5 mL) at room temperature was added triethylamine (0.16 mL, 1.2 mmol) and benzenesulfonyl chloride (0.11 mL, 0.82 mmol). The resultant mixture was stirred at room temperature overnight. The solvent was evaporated and the residue purified by prep TLC eluting with 2:1 hexanes/EtOAc to yield N-[4-[5-amino-1(4-methylphenyl)-1H-pyrazol-3-yl]phenyl]-N-(phenylsulfonyl)-benzenesulfonamide as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531478B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-6d05c43c20f94048a4fdf81d50ae0e74 |
| Source note | uspto-grants-2003_03 |