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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80532Generated: October 30, 2026

Potassium Carbonate → N-[5-(4-bromophenyl)-1,3,4-thiadiazol-2-yl]-4-chlorobutanamide

https://huagongshe.com/reaction/80532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant5-(4-Bromophenyl)-1,3,4-thiadiazol-2-amineHCID 554215—
SolventTolueneHCID 1140—
ProductN-[5-(4-bromophenyl)-1,3,4-thiadiazol-2-yl]-4-chlorobutanamideHCID 347548487%

Reaction Steps

A mixture of 5-(4-bromophenyl)-1,3,4-thiadiazol-2-amine (10.2 g, 0.04 mol), 4-chlorobutyryl 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 (12.5 g, 87% yield), mp 187-9° C., m/e 360, 15.7% (consistent with molecular formula C12H11BrClN3OS, calcd. 360.66). 1H NMR (DMSO-d6): δ 1.96-2.22 (m, 2H, —CH2), 2.69-2.81 (m, 2H, —CH2), 3.71-3.72 (m, 2H, —CH2), 7.49-7.88 (dd, 4H, ArH), 12.76 (br s, 1H, NH). 13C NMR: δ 27.3, 32.1, 44.6, 123.8, 128.7, 129.4, 132.3, 158.5, 160.7, 170.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846665B2
Source datasetuspto-grants-2014_09
ORD IDord-9da5ff71e88645ccaa44b1c3a0cae9bf
Source noteuspto-grants-2014_09