HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 18385416, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 12243795 | HCID 12243795 | — |
| Reactant | HCID 18385438 | HCID 18385438 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 18385416 | HCID 18385416 | 79% |
Reaction Steps
A solution of 3-(azidocarbonyl)-1-(ethoxycarbonyl)indole prepared according to Suvorov (ibid) (1.32 g, 5.12 mmol) in benzene (25 ml) was heated to reflux for 7 hours. After cooling to room temperature. THF (25 ml) and [2-(3-indolyl)-2-oxoethyl]ammonium bromide [Oikawa,Y. et al. Heterocycles 12 (1979) 1457-1462] (1.31 g, 5.12 mmol) were added immediately followed by ethyldiisopropylamine (0.89 ml, 5.12 mmol). After stirring for 1.5 hours the formed precipitate was removed by filtration and washed with THF followed by water. The sub-title compound (1.65 g, 79%) was obtained as a white solid after drying.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492409B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-702c402fe3ac40a8a8f17f801d533fa0 |
| Source note | uspto-grants-2002_12 |