HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980683Generated: October 29, 2026
Cysteamine Hydrochloride → HCID 178494333, compound
https://huagongshe.com/reaction/1980683
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(Chloromethyl)-4-methyl-1,3-thiazole | HCID 11275091 | — |
| Reactant | 3,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxide | HCID 12230538 | — |
| Reactant | (4-Methyl-1,3-thiazol-2-yl)methanol | HCID 17750909 | — |
| Product | HCID 178494333 | HCID 178494333 | — |
Reaction Steps
When 2-chloromethyl-4-methylthiazole [prepared by the reaction of thionyl chloride and 2-hydroxymethyl-4-methylthiazole, which itself is prepared according to the procedure of J. Chem. Soc., (Suppl. Issue No. 1), S106-111 (1966) or Acta Chem. Scand., 20, 2649 (1966)] is reacted with cysteamine hydrochloride and about two equivalents of a strong base such as sodium methoxide, and the resultant amine is treated with 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide, there is produced 3-methoxy-4-{2-[(4-methylthiazol-2-yl)methylthio]ethylamino}-1,2,5-thiadiazole 1,1-dioxide. When the latter compound is reacted with methylamine according to the general procedure of Example 31, there is produced 3-methylamino-4-{2-[(4-methylthiazol-2-yl)methylthio]ethylamino}-1,2,5-thiadiazole 1,1-dioxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04510309 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-9dc2b37d0f734b5ebe05716143845e9d |
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| Source note | uspto-grants-1985_04 |
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