HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-chloro-1-methyl-1H-pyrrolo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Chloro-1H-pyrrolo[2,3-c]pyridine | HCID 11435048 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-chloro-1-methyl-1H-pyrrolo[2,3-c]pyridine | HCID 59424476 | 92% |
Reaction Steps
To a solution of 259 (250mg, 1.64 mmol) in DMF (16 mL) at 0° C. was added NaH (197 mg, 4.92 mmol, 60% in mineral oil), and the mixture was stirred for 30 min, followed by addition of Mel (112 □L, 1.80 mmol). The reaction mixture was stirred at room temperature for 2 h before acetic acid (1 mL) was added. Solvents were removed under reduced pressure, the residue was partitioned between water and EtOAc. Organic phase was collected, dried over anhydrous Na2SO4 and concentrated. The residue was purified by flash column chromatography, eluent EtOAc/hexane (1:1), to afford the title compound 263 (200 mg, 92% yield) as an off-white solid. MS (m/z): 167.1(M+H) (found).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772247B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-1aaada9a5f964226bd5f1ccd4d700ad5 |
| Source note | uspto-grants-2010_08 |