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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855461Generated: October 30, 2026

2-Amino-4,6-dimethyl pyrimidine → HCID 44193377, compound

https://huagongshe.com/reaction/1855461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethyl pyrimidineHCID 13021—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantPhenolate SodiumHCID 4445035—
Reactant5-bromo-2-(4-methyl-1H-imidazol-1-yl)benzonitrileHCID 66961517—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 44193377HCID 44193377—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-bromo-2-(4-methyl-imidazol-1-yl)-benzonitrile (200 mg, 0.76 mmol), 2-amino-4,6-dimethyl-pyrimidine (141 mg, 1.14 mmol), sodium phenoxide (266 mg, 2.29 mmol), tris(dibenzylideneacetone)dipalladium chloroform complex (21 mg, 0.02 mmol) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene=xanthphos (26 mg, 0.04 mmol) in 5 mL of dioxane was heated to 80° C. under argon for 2 hours. The mixture was diluted with water, extracted with ethyl acetate and the product purified by by chromatography on silica gel using dichloromethane/methanol 9:1 v/v as an eluent. The title compound was obtained as a colorless solid (144 mg, 62%). MS ISP (m/e): 305.1 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): 8 (ppm)=10.08 (s, 1H), 8.44 (s, 1H), 8.15 (d, 1H), 7.89 (s, 1H), 7.55 (d, 1H), 7.25 (s, 1H), 6.76 (s, 1H), 2.36 (s, 6H), 2.18 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-9aa26a655ce440f9b513a83edf4d4213
Source noteuspto-grants-2015_02