HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10442179, compound → HCID 9951324, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10442179 | HCID 10442179 | — |
| Reactant | HCID 21184334 | HCID 21184334 | — |
| Product | HCID 9951324 | HCID 9951324 | 47.6% |
Reaction Steps
A methanolic solution of 1-N-glycidylindole (0.52 g, 3.0 mmole) from example 4 and 3-(4-tetrahydropyridinyl)indole (0.59 g, 3.0 mmole) was refluxed under nitrogen for 24 hours. The reaction mixture was concentrated in vacuo and the product purified by flash silica gel chromatography (ethyl acetate) to afford the titled compound as a yellow colored solid (0.53 g, 47% yield). Treatment with a 0.25M ethanolic solution of fumaric acid (0.5 equivalents) gave the required product as a yellow colored solid. The product was recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06204274B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-cb44ea4541114734aba5d92400839ba4 |
| Source note | uspto-grants-2001_03 |