HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine hydrochloride → HCID 53902970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 14347892 | HCID 14347892 | — |
| Reactant | HCID 19837869 | HCID 19837869 | — |
| Product | HCID 53902970 | HCID 53902970 | — |
Reaction Steps
For example, when sodium (or potassium) ethylmercaptide was used in place of the sodium methylmercaptide in Step A, one obtained (2S, 3R, 4R)-5-(ethylthio)-3-hydroxy-4-methyl-2-(methylamino)pentanoic acid. Likewise, when the methylamine hydrochloride of Step H was replaced by ammonium chloride, (2S, 3R, [4R]4S)-2-amino-3-hydroxy-4-methyl-5-(methylthio)-pentanoic acid was obtained, and when ethylamine hydrochloride was used, (2A, 3R, [4R]4S)-2-(ethylamino)-3-hydroxy-4-methyl-5-(methyl-thio)pentanoic acid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798823 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-f23d690013e24136862411c2c7809c5f |
| Source note | uspto-grants-1989_01 |