HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 68996976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Methyl-1H-pyrrole-2-carbonyl chloride | HCID 2795092 | — |
| Reactant | 2-[2-(1H-indazol-3-yl)vinyl]-4-(morpholin-4-yl)phenylamine | HCID 69004300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68996976 | HCID 68996976 | — |
Reaction Steps
2-[2-(1H-indazol-3-yl)vinyl]-4-(morpholin-4-yl)phenylamine (0.30 g, 0.94 mmol) synthesized in Example 225 was dissolved in THF (10 mL) and the solution was added with triethylamine (0.40 mL, 2.9 mmol) and N-methylpyrrolecarbonyl chloride (0.41 g, 2.8 mmol), followed by stirring at room temperature for 1 hour. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate solution, extracted with ethyl acetate and the organic layer was concentrated under reduced pressure to obtain free base of Compound 226. Further, said free base was treated by 4 mol/L hydrogen chloride-methanol solution (1.0 mL) to obtain Compound 226 (0.23 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605272B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-45e5a1e66fe14058a5dcdaa2fdd255ec |
| Source note | uspto-grants-2009_10 |