HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1S)-(+)-Camphor-10-sulphonic acid → 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1S)-(+)-Camphor-10-sulphonic acid | HCID 218580 | — |
| Reactant | 5-bromo-2,3-dihydro-1H-inden-2-amine | HCID 11298795 | — |
| Product | 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)- | HCID 11275870 | — |
| Product | (r)-5-bromo-2-aminoindan (1S)-(+)-10-camphorsulfonate salt | HCID 86588388 | — |
Reaction Steps
The title compound was prepared using a similar method to that described in Prashad et al, Adv. Synth. Catal. 2001, 343, No. 5, pp 461-472: ie by resolution of the free base form of racemic 5-bromo-2-aminoindan using (1S)-(+)-10-camphorsulphonic acid to obtain (R)-5-bromo-2-aminoindan (1S)-(+)-10-camphorsulfonate salt. The enantiomeric purity of (R)-5-bromo-2-aminoindan (1S)-(+)-10-camphorsulfonate salt was checked by HPLC using the following conditions:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618969B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-5acb0318df6347bf976386cbfec323ac |
| Source note | uspto-grants-2009_11 |