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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731496Generated: October 25, 2026

Methylamine → 5-amino-N-methyl-1,3,4-thiadiazole-2-sulfonamide

https://huagongshe.com/reaction/731496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant5-(Acetylamino)-1,3,4-thiadiazole-2-sulfonyl chlorideHCID 12894451—
SolventTetrahydrofuranHCID 8028—
Product5-amino-N-methyl-1,3,4-thiadiazole-2-sulfonamideHCID 67483682—

Reaction Steps

Methylamine (2M in THF, 40 mmol) was added to a suspension of 5-acetylamino-1,3,4-thiadiazole-2-sulfonyl chloride (10 mmol) (prepared as described in Bioorg. Med. Chem. 5, 515, 1997) in THF (10 mL) at −20° C. The mixture was stirred at room temperature over night and evaporated to dryness. The crude methylsulfonamide was suspended in EtOH (15 mL) and added 4N HCl in dioxane (15 mL) and heated for 4 h at 80° C. and then cooled to room temperature and evaporated to dryness to give crude 5-amino-1,3,4-thiadiazole-2-sulfonic acid methylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582769B2
Source datasetuspto-grants-2009_09
ORD IDord-182dba6a50ef45dc97d03ccfdac3c922
Source noteuspto-grants-2009_09