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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404708Generated: October 25, 2026

Potassium Bromide → HCID 66613626, compound

https://huagongshe.com/reaction/1404708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantN-methyl-5-(pyridin-3-yl)-1,3,4-thiadiazol-2-amineHCID 6488196—
Reactant4-Oxopentanoyl chlorideHCID 12300406—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 66613626HCID 66613626—

Reaction Steps

4-oxopentanoyl chloride (0.378 g, 2.8 mmol) was added to a suspension of N-methyl-5-(3-pyridyl)-1,3,4-thiadiazol-2-amine (0.3 g, 1.6 mmol) and 4-N,N-dimethylaminopyridine (0.229 g, 1.9 mmol) in dichloroethane (5 mL), stirred under nitrogen at room temperature for 30 minutes, refluxed for 14 hours, cooled, diluted with dichloroethane (50 mL) and washed with saturated aqueous sodium bicarbonate (70 mL). The aqueous layer was extracted with dichloroethane (30 mL) and the combined organic layers were dried over MgSO4, adsorbed on silica, applied to a Michel-Miller column and eluted with 9:1 ethyl acetate/hexane. The major fraction was collected and recrystallized from ethyl acetate/hexane to afford yellow needles. Yield 0.21 g (46%): mp 146-147° C.; IR (KBr, thin film) 1701, 1659 cm−1; 1HNMR (400 MHz, CDCl3) δ 9.13 (d, J=1.8 Hz, 1H), 8.69 (dd, J=4.8, 1.5 Hz, 1H), 8.28 (dt, J=6.2, 1.9 Hz, 1H), 7.42 (dd, J=8.0, 5.1 Hz, 1H), 3.90 (s, 3H), 2.96 (br, 4H), 2.29 (s, 3H); ESIMS m/z 291 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912338B2
Source datasetuspto-grants-2014_12
ORD IDord-27d3ef8f2c2c4ec0a83e0546bc80e6be
Source noteuspto-grants-2014_12