HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702381Generated: October 29, 2026
Cysteamine Hydrochloride → HCID 15592303, compound
https://huagongshe.com/reaction/1702381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | 2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole | HCID 3826620 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15592303 | HCID 15592303 | 110.8% |
Reaction Steps
Cysteamine hydrochloride (1.13 g; 0.01 mole) was added to a stirred solution of sodium methylate (1.08 g; 0.02 mole) in 20 ml of methanol at 0° under an argon atmosphere. The mixture was stirred for 1 hour at 0° and the resultant suspension was added dropwise over a period of 25 minutes to a stirred solution of 2-methyl-5-chloromethyl-1,3,4-oxadiazole (1.32 g; 0.01 mole) [prepared by the procedure described in Hel. Chim. Acta, 55, 1979 (1972)] in 15 ml of methanol at 0°. The reaction mixture was stirred at ambient temperature for 45 minutes, concentrated to near dryness, and then diluted with methylene chloride, filtered and evaporated under reduced pressure to give the title compound (1.92 g) as a yellow oil. The NMR spectrum (60 MHz) in CDCl3 gave the following resonances δ: 3.87 (s, 2H); 2.8 (m, 4H); 2.53 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04380639 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-f6513858b3ed4746b4b1ac89a065840c |
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| Source note | uspto-grants-1983_04 |
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