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. dioxan (50 mL) was stirred for 6 h at 80° C. The solvent was then removed in a vacuum, the residue mixed with CHCl3 (100 mL) and washed twice with water. The organic phase was dried over Na2SO4, concentrated to low volume in a vacuum, and the remaining residue purified by flash chromatography with CHCl3/MeOH (50:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977370B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-0e009ee5c1984fb5b250ce68b3a5de3e |
| Source note | uspto-grants-2011_07 |