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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415363Generated: October 29, 2026

Pyridine → HCID 178462381, compound

https://huagongshe.com/reaction/415363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantHCID 178462379HCID 178462379—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178462381HCID 17846238181%

Reaction Conditions

Temperature0 °C

Reaction Steps

KSCN (10.76 g, 110.7 mmol) and pyridine (3.9 mL, 49.2 mmol) was added to 6-amino-2-{[(1S)-1-(2-fluorophenyl)ethyl]thio}pyrimidin-4-ol (6.53 g, 24.6 mmol) in DMF (70 mL). The mixture was cooled to 0° C. and Br2 was added dropwise. After 3.5 h the reaction mixture was poured into water and the formed precipitate was collected by filtration. The solid was suspended in a mixture of DMF (75 mL) and water (15 mL) and heated to 120° C. for 8 h. The reaction mixture was poured into water and the solid was collected by filtration and dried in vacuo at 40° C. to give the title compound (6.42 g, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088780B2
Source datasetuspto-grants-2012_01
ORD IDord-dd48bad7186e444e8532d80ebd29139c
Source noteuspto-grants-2012_01