HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-{4-[3'-(4-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-N-methyl-methanesulfonamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 59321877 | HCID 59321877 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | N-(2-{4-[3'-(4-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-N-methyl-methanesulfonamide hydrochloride | HCID 68596214 | 97% |
Reaction Steps
Dissolve (2-{4-[3′-(4-fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-methyl-amine (0.124 g, 0.314 mmol) in DCM (3 mL) with triethylamine (66 μL, 0.470 mmol). Add methanesulfonyl chloride (26 μL, 0.329 mmol) dropwise in DCM (1 mL). Stir the mixture for 20 hr. Dilute with saturated aqueous sodium bicarbonate then extract 3 times with DCM. Dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 4.5:95.5 2 M ammonia in methanol:DCM), to give a yellow oil. Dissolve the oil in methanol and add ammonium chloride then sonicate the mixture for 10 min. Evaporate the solution to give the title compound as a yellow solid (0.154 g, 97%). MS (ES): m/z=474 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202873B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-0b1465dc6009492884cef2e16580b014 |
| Source note | uspto-grants-2012_06 |