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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215017Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 21948183, compound

https://huagongshe.com/reaction/2215017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
Reactant1,2,2,3-TetramethylpiperidineHCID 18761772—
ReactantHCID 21948150HCID 21948150—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418821HCID 178418821—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21948183HCID 2194818316.4%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of LTMP [freshly prepared at 0° C. from tetramethylpiperidine (785.4 mg, 5.6 mmol), TMEDA (651 mg, 5.6 mmol) and n-BuLi (3.5 mL, 5.6 mmol)] in THF (10 mL) was added to a cooled (−40° C.) stirred solution of 2-anilino-6-fluoro-7-methoxy-1-phenyl-1,8-naphthyridin-4(1H)-one (507 mg, 104 mmol) in THF (20 mL). The reaction mixture was warmed to room temperature. After 1 h, the mixture was cooled to −30° C. and 1,2-dibromotetrachloroethane (457 mg, 1.4 mmol) was added. After 30 min, water (50 mL) was added slowly, and then the reaction was warmed to room temperature and extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo. Silica gel flash chromatography of the residue using EtOAc afforded 2-anilino-5-bromo-6-fluoro-7-methoxy-1-phenyl-1,8-naphthyridin-4(1H)-one (101 mg, 16%) as a light yellow solid: LCMS RT: 2.75 min, MH+: 440.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109196B2
Source datasetuspto-grants-2006_09
ORD IDord-822237df4f8748fc865d5f336461f309
Source noteuspto-grants-2006_09