Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550761Generated: October 30, 2026

Pyridine → HCID 178462380, compound

https://huagongshe.com/reaction/550761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantHCID 178462378HCID 178462378—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178462380HCID 17846238065.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Pyridine (0.6 g, 7.6 mmol) was added to 6-amino-2-{[(1S)-1-phenylethyl]thio}pyrimidin-4-ol (1 g, 4 mmol) and KSCN (1.7 g, 16 mmol) in DMF (20 mL). The reaction mixture was cooled to 0° C. and bromine (0.65 g, 4.0 mmol) was then added in one portion. The reaction mixture was poured into water after 2 h and the orange precipitate was filtered off and washed with water. The solid was suspended in a mixture of DMF (6 mL) and water (2 mL) and heated to 110° C. After 30 h, the reaction mixture was poured into water, the yellowish precipitate was filtered off and washed with water and ether. The solid was dried in vacuum at 40° C. to give the title compound (0.8 g, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947693B2
Source datasetuspto-grants-2011_05
ORD IDord-e813ba49d5eb4907816221e16f1242de
Source noteuspto-grants-2011_05