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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902093Generated: October 31, 2026

Hydrochloric Acid → HCID 69314240, compound

https://huagongshe.com/reaction/902093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 58832865HCID 58832865—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 69314240HCID 69314240—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 8-(2-bromo-4-isopropyl-phenyl)-2-methyl-4-(1-propyl-butylamino)-pyrrolo[1,2-a]pyrimidine-6-carbonitrile (321 mg) in ethanol (1.5 mL) was added conc. HCl (0.75 mL) and heated for 50° C. for 3 hours. The reaction mixture was cooled to room temperature, poured into a saturated aqueous sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give crude product. To a solution of the crude product in ethyl acetate (2 mL) and ethanol (0.2 mL) was added 4M HCl/ethyl acetate (0.25 mL) under ice-cooling and concentrated under reduced pressure. The residue was crystallized from ethyl acetate to provide 4-(2-bromo-4-isopropyl-phenyl)-6-methyl-1-(1-propyl-butyl)-1H-1,5,7b-triaza-cyclopenta[cd]inden-2-ylideneamine hydrochloride (350 mg) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365078B2
Source datasetuspto-grants-2008_04
ORD IDord-d57582a17f0548d09bc3226020c6b52a
Source noteuspto-grants-2008_04