HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497792Generated: October 30, 2026
Methyl benzenesulfonate → {3-[6-[2-(4-Cyano-phenyl)-2H-pyrazol-3-yl]-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-propyl}-trimethyl-ammonium benzenesulfonate
https://huagongshe.com/reaction/1497792
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl benzenesulfonate | HCID 6630 | — |
| Reactant | 4-{5-[2-(3-Dimethylamino-propylamino)-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]-pyrazol-1-yl}-benzonitrile | HCID 73051920 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | {3-[6-[2-(4-Cyano-phenyl)-2H-pyrazol-3-yl]-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-propyl}-trimethyl-ammonium benzenesulfonate | HCID 73052080 | 89.3% |
Reaction Steps
To a solution of 4-{5-[2-(3-dimethylamino-propylamino)-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]-pyrazol-1-yl}-benzonitrile (Ex. 28, 55 mg, 0.10 mmol) in acetone (0.44 mL) was added methylbenzenesulfonate (15 μL, 0.11 mmol) at ambient temperature. The reaction mixture was heated 55° C. for 1.5 hrs. The cooled reaction mixture was concentrated in vacuo to give a clear colorless oil. The oil thus obtained was triturated in diethyl ether and the resultant solid taken up in minimal EtOAc and Et2O added until a white solid formed. The precipitate was collected by filtration, washed with Et2O and dried in vacuo to yield the title compound as a white solid (64 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199984B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-ff8a2e09e4314ed18a7442eb7c809a05 |
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| Source note | uspto-grants-2015_12 |
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