HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3-Iodo-1-methyl-2-pyridin-4-yl-1H-pyrrolo[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Dimethyl-(2-pyridin-4-ylethynyl-pyridin-3-yl)-amine | HCID 68429284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Iodo-1-methyl-2-pyridin-4-yl-1H-pyrrolo[3,2-b]pyridine | HCID 68430585 | 40.7% |
Reaction Steps
1 g (4.4 mmoles) of Dimethyl-(2-pyridin-4-ylethynyl-pyridin-3-yl)-amine are dissolved in 60 mL of dichloromethane under argon atmosphere. A solution of 2.27 g of iodine (8.9 mmoles) in 35 mL of dichloromethane is added dropwise in the reaction mixture at 0° C. The reaction mixture is allowed to reach room temperature and further stirred for 4 hours. The reaction mixture is then poured into a solution sodium thiosulfate and extracted with dichloromethane. The organic phase is washed with water and dried over magnesium sulfate. The solid residue after concentration is purified by chromatography on silica gel (ethylacetate) to give 600 mg of 3-Iodo-1-methyl-2-pyridin-4-yl-1H-pyrrolo[3,2-b]pyridine as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084395B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-0f92119da96a421f9e3b88b7f28a0351 |
| Source note | uspto-grants-2011_12 |