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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCysteamine HydrochlorideHCID 9082—
ReactantSodium HydroxideHCID 14798—
Reactant1-(4-(chloromethyl)thiazol-2-yl)-N,N-dimethylmethanamine hydrochlorideHCID 13121958—
SolventDichloromethaneHCID 6344—
Product2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468517
Source datasetuspto-grants-1984_08
ORD IDord-9a348502f595434ca75088b29493b1a4
Source noteuspto-grants-1984_08