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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489004Generated: October 31, 2026

Triethylamine → HCID 11171593, compound

https://huagongshe.com/reaction/1489004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantHCID 23303073HCID 23303073—
SolventDichloromethaneHCID 6344—
ProductHCID 11171593HCID 1117159392%

Reaction Conditions

Temperature0 °C

Reaction Steps

To solution containing 1-(butylcarbamoyl)-1,3-dihydroimidazole-2-thione (4.73 g, 23.7 mmole) suspended in 15 mL of dichloromethane cooled to 0° C. under a nitrogen atmosphere, was added bromine (3.79 g, 23.7 mmole) dissolved in 15 mL of dichloromethane, in a dropwise manner. After the addition was complete, triethylamine (4.81 g, 47.5 mmole) dissolved in 15 mL dichloromethane was added such that the temperature of the reaction mixture never exceeded 0° C. The reaction mixture was maintained at 0° C. for an additional 2 h and then stirred for 16 h at room temperature. It was then diluted with 150 mL of dichloromethane and washed twice with water and once with a saturated sodium chloride solution. The organic layer was then dried over magnesium sulfate and evaporated to dryness to yield 4.30 g (92%) of 2-butylimidazo[1,2-d]-1,2,4-thiadiazole-3(2H)-one as an off-white powder: mp 142°-143° C.; 1H NMR (CDCl3) δ7.40 (d, 1H), 7.20 (d, 1H), 3.79 (t, 2H), 1.73 (m, 2H), 1.40 (m, 2H), 0.957 (t, 3H) ppm; IR (KBr) ν1702 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677302
Source datasetuspto-grants-1997_10
ORD IDord-8b1846172f1f4549953929bac451d400
Source noteuspto-grants-1997_10