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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966199Generated: October 30, 2026

Benzoyl chloride → 1-(5-Bromopyridin-2-yl)thiourea

https://huagongshe.com/reaction/1966199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventAcetoneHCID 180—
Product1-(5-Bromopyridin-2-yl)thioureaHCID 2343887463%

Reaction Steps

1.1 Ammoniumthiocyanat (76 mmol, 1.2 eq.) is dissolved in acetone (75 ml) and benzoylchloride (1 eq.) is added dropwise. 20 min after stirring at RT, the reaction is heated to reflux. 2-Amino-5-bromopyridine (71 mmol) in acetone (50 ml) is added and 30 min heated to reflux. Afterwards, the reaction solution is poured onto ice. The precipitate is filtered and washed with water/methanol (1:1). The precipitate is dissolved in 2M NaOH (120 ml) at 80° C. and stirred 10 min at 80° C. The solution is poured into an HCl solution (5%) at 0° C. The pH of the solution is adjusted to 8 with a saturated Na2CO3 solution. The resulting precipitate is filtered and washed with water. (5-Bromo-pyridine-2-yl)-thiourea (“1”) is obtained after drying in vacuo at 40° C. as a pale yellow solid in a yield of 63%. HPLC (method C): 1.43 min; LC-MS (method A): 1.062 min, 231.95 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420642B2
Source datasetuspto-grants-2013_04
ORD IDord-45f04fb846a741a2a95b2a68088b532e
Source noteuspto-grants-2013_04