HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cysteamine Hydrochloride → 2-(2-Aminoethylthiomethyl)-4-methoxypyridine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(Chloromethyl)-4-methoxypyridine hydrochloride | HCID 13923368 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Aminoethylthiomethyl)-4-methoxypyridine dihydrochloride | HCID 20474232 | 77.2% |
Reaction Steps
Cysteamine hydrochloride (7.62 g) was added to a solution of sodium (4.70 g) in ethanol (170 cc) and the mixture was stirred and cooled to 10° and 2-chloromethyl-4-methoxypyridine hydrochloride (11.5 g) in methanol (50 cc) was added over 35 minutes, and the mixture was left overnight at room temperature. The mixture was filtered and the filtrate was evaporated to a residue which was partitioned between chloroform and water. The chloroform extract was evaporated to an oil which was crystallised from 2.1M ethanolic hydrogen chloride to give 2-(2-aminoethylthiomethyl)-4-methoxypyridine dihydrochloride (12.4 g) m.p. 172.5° (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156727 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-415c4cc653844124bbadfcf21bdd18e7 |
| Source note | uspto-grants-1979_05 |