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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629200Generated: October 26, 2026

Diisopropylamine → 4,6-Dichloro-1-hydroxyfuro[3,4-c]pyridin-3(1H)-one

https://huagongshe.com/reaction/629200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
Reactantn-Butyl lithiumHCID 61028—
Reactant2,6-Dichloronicotinic acidHCID 854047—
SolventDimethylformamideHCID 6228—
Product4,6-Dichloro-1-hydroxyfuro[3,4-c]pyridin-3(1H)-oneHCID 89972412—

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-Butyllithium (46.7 ml) was added to 100 ml of THF at −78° C., followed by the addition of diisopropylamine (16.65 ml) over 15 min. The mixture was stirred for 1 h at −78° C., then 2,6-dichloronicotinic acid (7.12 g) was added over 10 min. Stirring at −78° C. was continued for 2 h, then DMF (23.26 ml) was added dropwise maintaining the T<−70° C. The mixture was stirred for 1 h at −78° C., warmed to −50° C. for 30 min, and allowed to warm to RT. The mixture was quenched carefully by the addition of 2 N HCl (167 ml) until acidic pH was reached. The mixture was extracted with EtOAc, the organic layers were washed with brine and dried over MgSO4. After evaporation of the solvents the crude material was used without further purification: brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315500B2
Source datasetuspto-grants-2016_04
ORD IDord-64a76638ddaa4f728e0261e764fb8397
Source noteuspto-grants-2016_04