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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716816Generated: October 31, 2026

Hydrochloric Acid → HCID 72700318, compound

https://huagongshe.com/reaction/716816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetonitrileHCID 6342—
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
ReactantHCID 71491180HCID 71491180—
CatalystIronHCID 23925—
SolventEthyl AcetateHCID 8857—
ProductHCID 72700318HCID 7270031833%

Reaction Steps

To a solution of spiro[1H-isobenzofuran-3,1′-cyclobutane]-5-ol (Intermediate 24, 50 mg, 0.28 mmol) in dry acetonitrile (4 mL) dipotassium carbonate (58.8 mg, 0.43 mmol) and then 2-chloro-5-nitro-pyrimidine (43.0 mg, 0.27 mmol) were added and the reaction mixture was stirred for 4 hours at room temperature. The reaction was diluted with ethyl acetate (20 ml) and washed with an aqueous saturated solution of ammonium chloride (2×10 ml). The organic layer was dried (Na2SO4), filtered and evaporated. The residue was dissolved in ethanol (5 mL)/water (1 mL). Iron (95.0 mg, 1.7 mmol) and an aqueous 6M solution of hydrogen chloride (0.05 ml, 0.3 mmol) were added and the reaction mixture was stirred at 50° C. for 3 hours. The catalyst was filtered off and the solution was diluted with an aqueous saturated solution of NaHCO3 (10 ml) and extracted with ethyl acetate (2×15 ml). The organic layer was dried (Na2SO4), filtered and evaporated and the residue was purified by flash chromatography (Biotage system) on silica gel using a SNAP 10 g as column and cyclohexane/ethyl acetate from 60:40 to 0:100 as eluent affording the title compound (24 mg) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193704B2
Source datasetuspto-grants-2015_11
ORD IDord-a908009f4217425c8c6d6d26fc1b6f92
Source noteuspto-grants-2015_11