HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 3-Bromo-5-methyl-1-tosyl-1h-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1H-Pyrrolo[2,3-B]pyridine, 5-methyl-1-[(4-methylphenyl)sulfonyl]- | HCID 49758924 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-5-methyl-1-tosyl-1h-pyrrolo[2,3-b]pyridine | HCID 49758979 | 99% |
Reaction Steps
5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridine (1.9 g, 6.62 mmol) in dichloromethane (40 mL) was treated dropwise with a solution of bromine (0.678 mL, 13.24 mmol) in dichloromethane (3 mL). The resulting solution was stirred at room temperature for 3 hours. The reaction mixture was partitioned between dichloromethane (150 mL) and a 1:1 mixture of a saturated aqueous solution of NaHCO3 and a saturated aqueous solution of Na2S2O3 (250 mL). The organic phase was separated and the aqueous phase was re-extracted twice with DCM (50 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo to give the desired compound as an off-white solid (2.381 g, 99% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530489B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-0d04107c40074aedadb2a7cc25d12507 |
| Source note | uspto-grants-2013_09 |