HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744255Generated: October 26, 2026
N-Acetyl-L-leucine → (1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-amine
https://huagongshe.com/reaction/1744255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Acetyl-L-leucine | HCID 70912 | — |
| Reactant | 5-tert-butyl-2,3-dihydro-1H-inden-1-amine | HCID 11506601 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-amine | HCID 24777891 | — |
Reaction Steps
5-tert-Butyl-2,3-dihydro-1H-inden-1-ylamine (25.51 g, 93% potency), N-acetyl-(L)-leucine (23.34 g), and methanol (315 mL) were combined and heated at 65° C. for 1 hour. The solution was allowed to cool to ambient temperature. The solids were filtered and washed with toluene. The solid was then resuspended in methanol (125 mL) and brought to reflux. The solution was allowed to cool to ambient temperature and the solids were filtered. The solid was dried at 40° C. under reduced pressure to provide the title compound (98.7% ee).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07015233B2 |
|---|
| Source dataset | uspto-grants-2006_03 |
|---|
| ORD ID | ord-1a66fd9681af4e0cbbb2daeb50635822 |
|---|
| Source note | uspto-grants-2006_03 |
|---|