HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-phenyl-1H-pyrrolo[3,2-c]pyridine → N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-phenyl-1H-pyrrolo[3,2-c]pyridine | HCID 58975078 | — |
| Reactant | 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride | HCID 58975125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamide | HCID 58975231 | 79% |
Reaction Steps
Add a 5 ml THF solution of 3-Phenyl-1H-pyrrolo[3,2-c]pyridine (500 mg, 2.57 mmol, 1 eq) to a 4 ml THF solution of KotBu (303 mg, 2.70 mmol, 1.05 eq) under N2 atmosphere. Stir reaction for 10 minutes and then add a 5 ml THF solution of 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (844 mg, 2.57 mmol, 1 eq). Stir reaction for 16 hours, remove solvent on rotovap, and purify by silica gel chromatography to give N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamide (982 mg, 79% yield). Mass Spectrum (m/e): 485.96 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276516B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-6852156c72714cedb8576b694088d6e5 |
| Source note | uspto-grants-2007_10 |