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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261441Generated: November 1, 2026

N-Nitro-S-methylisothiourea → HCID 178512642, compound

https://huagongshe.com/reaction/261441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Nitro-S-methylisothioureaHCID 135927615—
ReactantHCID 178512644HCID 178512644—
SolventEthanolHCID 702—
ProductHCID 178512642HCID 178512642—

Reaction Steps

To a solution of 2-guanidino-4-(4-aminobutyl)thiazole (0.426 g.) in ethanol (10 ml.) was added 2-methyl-1-nitroisothiourea (0.270 g.). The mixture was heated under reflux for 4 hours, allowed to cool to room temperature, evaporated to dryness and the residue triturated with alcohol. The product was filtered off and dried to give 2-guanidino-4-[4-(2-nitroguanidino)butyl]thiazole, m.p. 180°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04165377
Source datasetuspto-grants-1979_08
ORD IDord-4cbbf2d8d76840d6818dbab559e602f9
Source noteuspto-grants-1979_08