HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cysteamine Hydrochloride → 2-(2-Aminoethylthiomethyl)-3-ethoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Chloromethyl-3-ethoxypyridine hydrochloride | HCID 20474185 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Aminoethylthiomethyl)-3-ethoxypyridine | HCID 20402236 | 89.5% |
Reaction Steps
Cysteamine hydrochloride (2.76 g) was added to a stirred mixture of sodium (1.576 g) in ethanol (75 cc) at 12°, 2-Chloromethyl-3-ethoxypyridine hydrochloride (4.60 g) in ethanol (70 cc) was added over 30 minutes to this mixture stirred at 10°-12°. The mixture was left to stand overnight, filtered and the filtrate was evaporated to dryness. The residue was dissolved in water, acidified to pH 4 with hydrochloric acid and extracted with chloroform (discarded). The aqueous phase was adjusted to pH 12 with aqueous sodium hydroxide and was extracted with chloroform. The chloroform extracts were evaporated to give 2-(2-aminoethylthiomethyl)-3-ethoxypyridine (4.2 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04215126 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-3fefe612ee9c446eb6be068f01453351 |
| Source note | uspto-grants-1980_07 |