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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507611Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 60204508, compound

https://huagongshe.com/reaction/507611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-fluoropyrimidineHCID 583466—
ReactantHCID 60204507HCID 60204507—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductHCID 60204508HCID 60204508—

Reaction Conditions

Temperature-78 °C

Reaction Steps

8.4 mL (13 mmol) of a 1.6 M solution of tBuLi in heptane was added to a rapidly stirred suspension of 2.5 g (12 mmol) of N-(4-fluorophenyl)-N-methylthiazol-2-amine in 50 mL of THF at −78° C. The solution was stirred for 1 min at −78° C. before 1.3 mL (13 mmol) of 2-chloro-5-fluoropyrimidine was added. The reaction solution was stirred for 1 h at −78° C., then quenched by addition of 2 mL of MeOH. Solid 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (5.5 g, 24 mmol) was added and the reaction solution was stirred for 1 h and then 25 mL of 10% (w/v) aqueous NaOH was added. The reaction solution was warmed to rt and stirred 2 h, then poured into 500 mL of EtOAc and 200 mL of water, separated and the organic layer washed twice with saturated aqueous NaHCO3, once with brine, dried over MgSO4, filtered and concentrated. The residue was purified by C-18 prep MPLC to give the title compound. MS (M+H)+ 339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-651b588387ba44d8995dc66d730494d1
Source noteuspto-grants-2010_08