HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358528Generated: October 30, 2026
Water → 2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazole
https://huagongshe.com/reaction/358528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(4-(chloromethyl)thiazol-2-yl)-N,N-dimethylmethanamine hydrochloride | HCID 13121958 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazole | HCID 10977318 | — |
Reaction Steps
To the aqueous phase from Example 14 above was added 27 g. of 2-aminoethanethiol, hydrochloride. The mixture was heated and stirred, until the pot temperature reached 120°. The mixture was held at that temperature for 6 hours, and was then allowed to cool to 60°. To the residue was added 80 ml. of deionized water, and the mixture was allowed to cool to ambient temperature and stand for some days. Eighty ml. of dichloromethane was then added, and the pH of the mixture was adjusted to 6.1 by the addition of 9 ml. of 50% sodium hydroxide. The aqueous layer was extracted twice with 40 ml. portions of dichloromethane, and the aqueous layer was then mixed with 80 ml. of dichloromethane and the pH was adjusted to 12.6 by the addition of 40 ml. of 50% sodium hydroxide. The aqueous layer of the resulting mixture was extracted twice with 40 ml. of dichloromethane, and the two aqueous layers were combined, filtered and evaporated under vacuum to obtain 31.5 g. of the desired product, which was found to be 74.7% pure by the analytical method described in Preparation 1 above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04468517 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-9a348502f595434ca75088b29493b1a4 |
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| Source note | uspto-grants-1984_08 |
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