HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorophenol → HCID 66917887, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorophenol | HCID 8449 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N,N-Dimethylglycine hydrochloride | HCID 75605 | — |
| Reactant | 7-Bromo-5-fluoro-3-methyl-1H-indole | HCID 53401203 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66917887 | HCID 66917887 | 34% |
Reaction Steps
Following general method A-18, 7-Bromo-5-fluoro-3-methyl-1H-indole (1.60 g, 7.02 mmol) was reacted with 2,4-dichlorophenol (1.72 g, 10.5 mmol), CuI (134 mg, 0.702 mmol), N,N-dimethylglycine hydrochloride (293 mg, 2.10 mmol), and Cs2CO3 (4.57 g, 14.0 mmol) in anhydrous dioxane (14 mL). The crude product was purified by silica gel column chromatography utilizing a solvent system of 5% EtOAc/Hexanes to yield 746 mg of I-198B as a yellow oil (34%). 1H NMR (400 MHz, CDCl3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07598397B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-bb2870dcaced4465a2ece16da8a84cff |
| Source note | uspto-grants-2009_10 |