HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15248974, compound → HCID 9800355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15248974 | HCID 15248974 | — |
| Reactant | HCID 21184334 | HCID 21184334 | — |
| Product | HCID 9800355 | HCID 9800355 | 9% |
Reaction Steps
A methanolic solution of 1-N-glycidyl-2-methylbenzimidazole (0.64 g, 3.4 mmole) from example 7 and 3-(4-tetrahydropyridinyl)indole (0.67 g, 3.4 mmole) was refluxed under nitrogen for 24 hours. The reaction mixture was concentrated in vacuo and the product purified by flash silica gel chromatography (10% methanol in ethyl acetate) to afford the titled compound as a pale yellow colored solid (0.11 g, 9% 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-5effe5aea33d40f4aa3090e46821d178 |
| Source note | uspto-grants-2001_03 |