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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894310Generated: October 30, 2026

Methanesulfonamide → HCID 178505163, compound

https://huagongshe.com/reaction/894310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
ReactantMethyl 3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]propanimidateHCID 12881442—
SolventMethanolHCID 887—
ProductHCID 178505163HCID 17850516392.1%

Reaction Steps

In 10.2 ml of methanol were dissolved 1.27 g of methyl 3-[(2-guanidinothiazol-4-yl)methylthio]propionimidate and 0.86 g of methanesulfonamide and after reacting for 48 hours at room temperature, the solvent was distilled off under reduced pressure. Then, the residue formed was purified by a silica gel column chromatography using a mixture of chloroform and methanol (20:1→10:1) to provide 1.44 g amorphous 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-346f90de3eff4283acb88e9e7f6c2cd3
Source noteuspto-grants-1981_08