HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1S,2R)-2-Aminocyclopentane-1-carboxylic acid → rel-(1R,2S)-2-Amino-N-(1-methylethyl)cyclopentanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1S,2R)-2-Aminocyclopentane-1-carboxylic acid | HCID 73306 | — |
| Reactant | Cyclopentanecarboxylic acid, 2-amino- | HCID 429614 | — |
| Product | rel-(1R,2S)-2-Amino-N-(1-methylethyl)cyclopentanecarboxamide | HCID 24896496 | — |
Reaction Steps
The chiral compound (1S,2R)-2-aminocyclopentane-carboxylic acid isopropylamide is prepared analogously to this procedure using (1S,2R)-2-aminocyclopentanecarboxylic acid. In addition, a number of amides are prepared in this way starting from 2-aminocyclopentanecarboxylic acid (racemic or chiral).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623887B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-08b49b5347d64940ad9234f627bae746 |
| Source note | uspto-grants-2014_01 |