HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096263Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 59564416, compound
https://huagongshe.com/reaction/2096263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | HCID 59548846 | HCID 59548846 | — |
| Product | HCID 59564416 | HCID 59564416 | 89.4% |
Reaction Steps
The N-(2-amino-phenyl)-2-{4-[2-(3,5-dimethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzamide (0.050 g, 0.116 mmol) is dissolved into 2 mL of dichloroethane and placed in a microwave tube. To this is added a catalytic amt. of p-TsOH. The mixture is heated in a microwave at 130° C. for 20 min and then 160° C. for 30 min. The reaction mixture is concentrated to dryness and the product is purified using a Gilson Prep HPLC system eluting with 20%-100% CH3CN/H2O) to give 43 mg of desired product. Impure fractions are concentrated and purified using a SiO2 prep plate eluting with (5% MeOH/CH2Cl2) to give an additional 17.5 mg of 1-{4-[2-(1H-benzoimidazol-2-yl)-phenyl]-piperazin-1-yl}-2-(3,5-dimethyl-pyrazol-1-yl)-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450317B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1cc6124ad1184e5087b7ea832a31974e |
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| Source note | uspto-grants-2013_05 |
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