HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22393210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-4-piperidinecarboxamide | HCID 22393167 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22393210 | HCID 22393210 | 47.6% |
Reaction Steps
A solution of N-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-4-piperidinecarboxamide (500 mg), benzyl bromide (370 mg) and potassium carbonate (300 mg) in dimethylformamide (10 ml) was stirred at 80° C. for 4 hours. The reaction mixture was poured into ice-water and extracted with chloroform. The residue obtained by water washing, drying and then concentration under reduced pressure was purified by silica gel column chromatography to give 300 mg of N-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyl-4-piperidinecarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218410B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-9f2955d9f8704f8d830facf62aca8f19 |
| Source note | uspto-grants-2001_04 |