HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoquinoline → HCID 10912790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10912790 | HCID 10912790 | — |
Reaction Steps
A solution of 3-(2-bromo-ethyl)-1H-indole (4.48 g, 20 mmol) and isoquinoline (5.33 g, 40 mmol) in abs. dioxane (50 ml) was stirred at 80° C. for 6 h. The solvent was then removed i. vac., CHCl3 (100 ml) was added to the residue and the mixture was washed twice with water. The organic phase was dried over Na2SO4 and concentrated i. vac. and the residue which remained was purified by flash chromatography with CHCl3/MeOH (50:1). Yield: 4.78 g (Ind-65, 86%), white solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138187B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-a54fc9215a98438d9294c81228e92574 |
| Source note | uspto-grants-2012_03 |