HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → HCID 59463816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 59463818 | HCID 59463818 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 59463816 | HCID 59463816 | 40.7% |
Reaction Steps
560 mg (1.7 mmol) of ethyl 3-(1-methoxy-5,6,7,8-tetrahydroisoquinolin-4-ylamino)benzoate (compound 12) are dissolved in 30 ml of chloroform and, at room temperature, 413 mg (2.1 mmol) of trimethylsilyl iodide are added. The mixture is then heated to reflux until complete conversion is reached by means of LCMS. Further trimethylsilyl iodide is added if necessary. For workup, the mixture is washed twice with H2O, dried with Na2SO4 and concentrated. Chromatography on silica gel (CH2Cl2/MeOH 95:5) affords 216 mg of the title compound. Yield: 40%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795278B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-d6c1ceb93baf4ecc89d6db11ec1d6e6e |
| Source note | uspto-grants-2010_09 |