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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420279Generated: November 1, 2026

N,N'-Dimethylethylenediamine → HCID 68554951, compound

https://huagongshe.com/reaction/420279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant2-PyrrolidoneHCID 12025—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 57386048HCID 57386048—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68554951HCID 68554951—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a solution of (3aR,7S,7aS)-7-(4-amino-3-fluoro-5-iodo-benzyl)-3-(3-tert-butyl-benzyl)-5,5-dioxo-hexahydro-1-oxa-5lambda*6*-thia-3-aza-inden-2-one (0.10 g, 0.17 mmol), 2-pyrrolidin-one (0.02 mL, 0.26 mmol) and N,N′-dimethylethylenediamine (0.002 mg, 0.017 mmol) in dioxane (10 mL) was added CuI (0.002 g, 0.009 mmol) and K3PO4 (0.077 g, 0.36 mmol) and the reaction mixture was heated at 115° C. for 4 h. The reaction mixture was filtered over Celite and concentrated. The crude product was purified on the flashmaster (10 g silicagel, cyclohexane-EtOAc 100:0 to 0:100) to yield the title compound as a yellow solid, which was directly used as such in the next step: HPLC RtC=4.728 min; ESIMS [M+H]+=544.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-6ad5d7d75bbe4d73a0a7e2568e5978a0
Source noteuspto-grants-2012_01