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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386819Generated: October 25, 2026

Diisopropylethylamine → 4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamide

https://huagongshe.com/reaction/386819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1,2,5-thiadiazole-3-carboxylic acidHCID 251763—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant3-Bromo-4-fluoroanilineHCID 2779286—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamideHCID 5855824476.8%

Reaction Steps

A solution of 4-amino-1,2,5-thiadiazole-3-carboxylic acid (250 mg, 1.7 mmol) and 3-bromo-4-fluoroaniline (393 mg, 2.1 mmol) in N,N-dimethylformamide (5 mL) was treated with O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (784 mg, 2.1 mmol) followed by N,N-diisopropylethylamine (0.36 mL, 2.1 mmol) and stirred for 16 h. The reaction mixture was diluted with brine (50 mL) and 0.1 N HCl (100 mL) and extracted with ethyl acetate (2×150 mL). The combined organic extracts were washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated. Purification of the crude reaction mixture on silica gel gave the desired product (414 mg, 76%). LCMS for C9H7BrFN4OS(M+H)+: m/z=316.9, 318.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372870B2
Source datasetuspto-grants-2013_02
ORD IDord-3787938b02ad40539dce4a9fc3ff1d74
Source noteuspto-grants-2013_02