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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850302Generated: October 25, 2026

1,2-Dichloroethane → 2,6-Dichloroquinazoline

https://huagongshe.com/reaction/1850302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantNitric acid, 1,1-dimethylethyl esterHCID 164756—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloroquinazolin-2-amineHCID 21183942—
Product2,6-DichloroquinazolineHCID 1241392820%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 6-chloro-quinazolin-2-ylamine (110) (2.8 g, 15.8 mmol) and SbCl3 (7.2 g, 32 mmol) in 1,2-dichloroethane (100 mL) was added tert-butylnitrate (6.2 ml, 52 mmol) and heated at 60° C. for 3 h under nitrogen atmosphere. To the mixture was added aqueous saturated NaHCO3 and the mixture was filtered off and filtrate was extracted with CHCl3. The organic layer was washed with brine, dried over Na2SO4, and evaporated. The residue was purified by silica gel column chromatography, using CHCl3/EtOAc (9:1, v/v) as eluent to give 2,6-dichloro-quinazoline (111) (0.65 g, 3.12 mmol, 20% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-114dc365ca4b49cbb0c43ace77126036
Source noteuspto-grants-2015_02