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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034594Generated: October 31, 2026

Thiophenol → 2-Amino-5-phenyl-3-phenylthiopyrazine

https://huagongshe.com/reaction/1034594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-5-phenylpyrazin-2-amineHCID 12453552—
SolventDimethylformamideHCID 6228—
Product2-Amino-5-phenyl-3-phenylthiopyrazineHCID 6684825279%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

To a cooled solution of thiophenol (0.10 mL, 1.00 mmol) in dry DMF (10 mL), sodium hydride (NaH) (0.025 g, 1.00 mmol) was added the resulting mixture was stirred for 15 min at 5-10° C. After this time 2-amino-3-bromo-5-phenylpyrazine 17b (0.25 g, 1.00 mmol) was added and the mixture refluxed for 20 h, cooled and extracted with EtOAc. The organic layer was washed with water, dried over Na2SO4, filtered and the solvent removed under reduced pressure to get a crude that was purified by flash chromatography using petroleum ether-EtOAc (60:40 v/v) as eluent, to obtain 0.22 g of the title compound 18b as a brown solid (mp 109-112° C., 79% yield). 1H-NMR (CDCl3): 4.92 (br s, 2H), 7.29-7.50 (m, 8H), 7.74-7.77 (m, 2H), 8.35 (s, 1H). MS (ESI): m/z 280 (M+H1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546147B2
Source datasetuspto-grants-2013_10
ORD IDord-46b8a61e9bfe45a89f2e453e6ad3bf2a
Source noteuspto-grants-2013_10