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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400368Generated: October 31, 2026

Potassium Carbonate → 4-chloro-N-(5-phenyl-1,3,4-thiadiazol-2-yl)butanamide

https://huagongshe.com/reaction/400368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant2-Amino-5-phenyl-1,3,4-thiadiazoleHCID 219408—
SolventTolueneHCID 1140—
Product4-chloro-N-(5-phenyl-1,3,4-thiadiazol-2-yl)butanamideHCID 841407585.2%

Reaction Steps

A mixture of 5-phenyl-1,3,4-thiadiazol-2-amine (7.1 g, 0.04 mol), 4-chloro-butyryl chloride (11.3 g, 9.0 ml, 0.08 mol) and potassium carbonate (5.5 g, 0.04 mole) in toluene (100 ml) was heated under reflux for 4 hr. The toluene was then evaporated under reduced pressure. The residue was then quenched with water, stirred, and filtered. The solid obtained was washed, dried and recrystallized from toluene to give the required product (9.6 g, 85% yield), mp 159-62° C., m/e 281, 87% (consistent with molecular formula C12H12ClN3OS, calcd. 281.04). 1H NMR (DMSO-d6): δ 2.07-2.10 (m, 2H, —CH2), 2.67-2.70 (m, 2H, —CH2), 3.70-3.72 (m, 2H, —CH2), 7.48-7.54 (m, 3H, ArH), 7.93-7.94 (m, 2H, ArH), 12.65 (br s, 1H, NH). 13C NMR: δ 27.9, 32.7, 45.1, 127.4, 129.8, 130.7, 131.0, 158.5, 162.4, 171.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741893B2
Source datasetuspto-grants-2014_06
ORD IDord-220eb16f95bd44ad8f5201597c5e3588
Source noteuspto-grants-2014_06