HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cysteamine → 3-(2-Aminoethylthio)-1-nonylpyrrolidine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cysteamine | HCID 6058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Nonylmaleimide | HCID 512831 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Aminoethylthio)-1-nonylpyrrolidine-2,5-dione | HCID 512847 | — |
Reaction Steps
A mixture of N-nonyl maleimide (0.01 M) prepared as described in Example 12 above, mercapto ethylamine (0.01 M) and triethylamine (0.001 M) in acetonitrile (50 ml) was stirred for 24 hours at room temperature. Acetonitrile was evaporated in vacuo and the residue obtained was triturated with ethyl acetate (25 ml). The resultant suspension was filtered and the solid washed with ethyl acetate. The solid was then dried and characterised as the desired product, N-nonyl,3-mercapto ethylamino maleimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476053B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-41389818c0f841dd979c4af0486aac44 |
| Source note | uspto-grants-2002_11 |