HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 67325813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamate | HCID 45073740 | — |
| Reactant | N-(3-amino-4-methylphenyl)-4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)benzamide | HCID 67324831 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67325813 | HCID 67325813 | 47% |
Reaction Steps
To a solution N-(3-amino-4-methylphenyl)-4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)benzamide (70 mg, 0.17 mmol) in DMF (0.5 mL) were added K2CO3 (69 mg, 0.50 mmol) and tert-butyl 5-(bromomethyl)pyrazin-2-ylcarbamate (48 mg, 0.17 mmol). The reaction mixture was stirred for 8 hours at room temperature after which, it was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash chromatography using (5% MeOH/CH2Cl2) as a solvent to afford title compound (50 mg, 47% yield). MS m/z: 628 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09180127B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-d7a55c2065d94f99b2b3cf71c47f1860 |
| Source note | uspto-grants-2015_11 |