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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808193Generated: October 25, 2026

Sodium Hydroxide → 4-[(1,2,4-Thiadiazol-5-ylamino)sulfonyl]benzoic acid

https://huagongshe.com/reaction/1808193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-Amino-1,2,4-thiadiazoleHCID 290274—
ReactantLithiumHCID 3028194—
ReactantMethyl 4-[(pentafluorophenoxy)sulfonyl]benzoateHCID 57732203—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[(1,2,4-Thiadiazol-5-ylamino)sulfonyl]benzoic acidHCID 5773221443%

Reaction Steps

To a solution of 5-amino-1,2,4-thiadiazole (58 mg, 0.574 mmol, 1.1 eq) in THF (5 ml) was added, 1,1,3,3,3-Hexanemethyldisilazane lithium salt (LiHMDS, 1M in THF, 1.15 ml, 1.2 mmol, 2.2 eq) and the reaction mixture stirred at 50° C. for 5 minutes. Methyl 4-[(pentafluorophenoxy)sulfonyl]benzoate (Preparation 28, 196 mg, 0.513 mmol, 1 eq) was added and the reaction monitored. On the disappearance of the starting materials the reaction mixture was quenched with water (5 ml), diluted with ethyl acetate (10 ml), washed with saturated sodium hydrogen carbonate, dried over sodium sulphate, filtered and evaporated in vacuo. The residue was dissolved in dioxane (5 ml) and a solution of sodium hydroxide (100 mg, 2.5 mmol, 4.3 eq) in water (2 ml) was added and the reaction mixture stirred at room temperature for 30 minutes. The reaction mixture was partitioned between ethyl acetate (5 ml) and water (5 ml), the aqueous phase was acidified with concentrated HCl, extracted into ethyl acetate (10 ml), dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was triturated with DCM to yield the title compound as a pale yellow solid (64 mg, 0.22 mmol, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-6798cc8ec440453b8848858464fee7a9
Source noteuspto-grants-2013_01