HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 68567915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 2-methyl-2-(pyridin-2-yl)propanoate | HCID 642856 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 57525626 | HCID 57525626 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 68567915 | HCID 68567915 | — |
Reaction Steps
A solution of trimethylaluminum in heptane (2.0 M, 19.5 mL) was added slowly to a solution of 2-tert-butyl-5-(3,3-dimethoxy-cyclobutyl)-2H-pyrazol-3-ylamine (8.98 g) in CH2Cl2 (60 mL) at room temperature. After 15 min, a solution of 2-methyl-2-pyridin-2-yl-propionic acid ethyl ester (6.85 g) in CH2Cl2 (60 mL) was added. The reaction mixture was heated to reflux overnight. Saturated aqueous NH4Cl solution was added and the mixture was extracted with CH2Cl2 (2×). The combined organic layers were dried over Na2SO4 and concentrated to afford N-[2-tert-butyl-5-(3,3-dimethoxy-cyclobutyl)-2H-pyrazol-3-yl]-2-pyridin-2-yl-isobutyramide as an oil that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671072B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-21fbfc68c1b44d2eb08e9d91898f5dec |
| Source note | uspto-grants-2010_03 |