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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048578Generated: November 4, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 58573923, compound

https://huagongshe.com/reaction/1048578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
ReactantHCID 67999073HCID 67999073—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium hydrogencarbonate brineHCID 129703874—
ProductHCID 58573923HCID 58573923—

Reaction Steps

To a solution of 3.09 g (4.33 mmol) N—((S)-2-((3R,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-(2-(4-methoxybenzyloxy)ethyl)-2-oxopiperidin-1-yl)butyl)-N-methylcyclopropanesulfonamide (Example 408, step C) in a mixture of DCM (82 mL) and water (4.56 mL) [18:1] was added 2,6-di-tert-butylpyridine (2.93 mL, 12.99 mmol) followed by DDQ (3.93 g, 17.32 mmol). The reaction mixture was stirred vigorously at ambient temperature for 15 min. The reaction mixture was diluted with 150 mL sat. NaHCO3/brine solution and extracted into 600 mL of ethyl acetate, then 200 mL of EtOAc×2 (precipitate was removed by filtration). The combined organic layers were dried over MgSO4, filtered and the filtrate was evaporated. Purification by chromatography on silica gel (eluent: 50-100%% EtOAc/hexane, gradient elution) provided the desired product as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-02c8e77ea4f74b6390468f4b1b152252
Source noteuspto-grants-2013_10