HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → N-(N-Acetyl-S-ethyl-L-cysteinyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | L-Cysteine, N-acetyl-S-ethyl- | HCID 147382 | — |
| Reactant | N-Acetyl-S-methyl-L-cysteine | HCID 13893975 | — |
| Product | N-(N-Acetyl-S-ethyl-L-cysteinyl)pyrrolidine | HCID 13048740 | — |
Reaction Steps
N-(N-Acetyl-S-ethyl-L-cysteinyl)pyrrolidine was synthesized in exactly the same manner as described in Example 14 except that the S-methyl-N-acetyl-L-cysteine and aqueous 70% ethylamine solution used in that example were replaced by S-ethyl-N-acetyl-L-cysteine and pyrrolidine, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440788 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-43770fb6fc084cfbb9825789b5f5b43d |
| Source note | uspto-grants-1984_04 |