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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670706Generated: October 31, 2026

Hydrochloric Acid → HCID 24771030, compound

https://huagongshe.com/reaction/1670706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-AminopyridineHCID 10439—
ReactantPerchloric AcidHCID 24247—
Reactant1-Isocyano-4-nitrobenzeneHCID 74802—
ReactantMethyl 2-formylbenzoateHCID 243003—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 24771030HCID 24771030338.2%

Reaction Steps

A mixture of 2-aminopyridine (I1) (1.0 equiv., 27.2 mmol, 3.00 g), 4-nitrophenyl isocyanide (1.1 equiv., 29.9 mmol, 4.40 g), methyl 2-formylbenzoate (1.1 equiv., 29.9 mmol, 4.9 g) and perchloric acid (0.2 equiv., 5.4 mmol, 0.55 g) in methanol was stirred at room temperature overnight. Potassium tert-butoxide (2.2 equiv., 59.8 mmol, 6.7 g) was added and the reaction mixture was further stirred at room temperature for 2 h. Acetic acid (2.0 ml) (or concentrated hydrochloric acid) was added, the resulting precipitate was filtered off and washed with isopropanol and isopropyl ether to give 9-hydroxy-6-(4-nitrophenyl)-pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5(6H)-one (10) (6.80 g, yield=67%, purity (LC)=95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994187B2
Source datasetuspto-grants-2011_08
ORD IDord-21bff4fcf27a41f9ae2b834738c5e2e1
Source noteuspto-grants-2011_08