HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58975180, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride | HCID 58975125 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58975180 | HCID 58975180 | 73% |
Reaction Steps
Add MeCN (2 ml) to a flask under N2 containing 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (50 mg, 0.152 mmol), 1H-pyrrolo[2,3-b]pyridine (18 mg, 0.152 mmol), 4-Pyrrolidin-1-yl-pyridine (2 mg, 0.167 mmol), and triethylamine (17 mg, 0.167 mmol). Heat reaction to 80° C. for 16 hours. Cool the solution to room temperature, remove MeCN on rotovap. Purify crude material on silica gel to give 45 mg (73% yield) of N-(4-Fluoro-benzyl)-4-(pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide. Mass Spectrum (m/e): 410.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595339B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-629d8914a3d0424185fd1cd220209027 |
| Source note | uspto-grants-2009_09 |