HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → HCID 59414580, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1-[(4-Methylphenyl)sulfonyl]-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine | HCID 49759030 | — |
| Solvent | Bicarbonate Ion | HCID 769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59414580 | HCID 59414580 | 89.1% |
Reaction Steps
To a stirred solution of 5-trifluoromethyl-1-tosyl-1H-pyrrolo[2,3-b]pyridine (53.7 g, 158 mmol) in DCM (250 mL) was added a solution of bromine (16 mL, 316 mmol) in DCM (50 mL) dropwise. No significant exotherm was observed. After an hour at room temperature, the reaction mixture had thickened and stirring ceased. The reaction was deemed complete by tlc and was diluted with 1.2 litres of DCM and 50:50 saturated bicarbonate: saturated sodium thiosulfate aqueous solution. The organic layer was separated and further washed with the 50:50 aqueous mixture, dried over magnesium sulfate and evaporated. The crude yellow solid was triturated with diethyl ether and solid isolated and dried to give the product as a yellow powder (59 g, 59% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530489B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-4cfe9585defc4ed3b5cd4936863335ab |
| Source note | uspto-grants-2013_09 |