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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894312Generated: October 30, 2026

Methanesulfonamide → HCID 178505163, compound

https://huagongshe.com/reaction/894312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
ReactantMethyl 3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]propanimidateHCID 12881442—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 178505163HCID 17850516356.9%

Reaction Steps

In 10 ml of methanol were dissolved 1 g of methyl 3-[(2-guanidinothiazol-4-yl)methylthio]propionimidate and 0.38 g of methanesulfonamide and after causing reaction for 48 hours at room temperature, the solvent was distilled off under reduced pressure. Then, the residue formed was dissolved in 3 ml of ethanol and the solution was allowed to cool, thereby white crystals deposited. The crystals were collected by filtration and dried to provide 0.7 g of N-methanesulfonyl-3-[(2-guanidinothiazol-4-yl)methylthio]propionamidine. The product shows the following physicochemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04283408
Source datasetuspto-grants-1981_08
ORD IDord-55f010669c4d48e5bb97bb7bc26f0921
Source noteuspto-grants-1981_08