HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356366Generated: October 29, 2026
1H,2H,3H,4H,5H,6H-azepino(4,5-b)indole → HCID 59075496, compound
https://huagongshe.com/reaction/1356366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H,2H,3H,4H,5H,6H-azepino(4,5-b)indole | HCID 27557 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 59075496 | HCID 59075496 | 68% |
Reaction Steps
A solution of 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (0.93 g, 5.0 mmol) in trifluoroacetic acid (17 mL) was cooled to 0° C., and treated with a freshly prepared solution of Na(CN)BH3 (1.57 g, 25 mmol) in MeOH (4 mL). The cooling bath was removed and the reaction mixture was stirred at room temperature for 1 h, then treated with water (75 mL), stirred for an additional 15 minutes before adjusting the pH to 14 with 45% KOH (aqueous). The resulting solution was extracted with EtOAc (3×40 mL), and the combined organic extracts were washed once with brine, dried over MgSO4, filtered, and concentrated in vacuo to give a yellow syrup. The crude product was purified by chromatography and using ethanol:ammonia:dichloromethane (15:1.5:83.5) and trituration of the resulting material gave the title compound (0.64 g) as an off-white solid: mp 102-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06586421B2 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-0ee4e68ba74d4f64936c7189c06d7255 |
|---|
| Source note | uspto-grants-2003_07 |
|---|