HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-phenyl-1H-pyrrolo[2,3-b]pyridine | HCID 52270684 | — |
| Reactant | 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride | HCID 58975125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide | HCID 57849045 | 18.5% |
Reaction Steps
Slowly add 3-phenyl-1H-pyrrolo[2,3-b]pyridine (178 mg, 0.915 mmol, 1.0 eq) as a 2 ml DMF solution to a flask under N2 containing potassium tertbutoxide (108 mg, 0.961 mmol, 1.05 eq) in 1 ml DMF solution. Stir solution for 5 minutes. Slowly add 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (300 mg, 0.915 mmol, 1.0 eq) as a 3 ml DMF solution. Stir reaction for 18 hours at room temperature. Strip reaction of solvent and purify on silica gel chromatography to give N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide (82 mg, 18% yield). Mass Spectrum (m/e): 485.94 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276516B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-e82320606cbb4546ad773905ac96c429 |
| Source note | uspto-grants-2007_10 |