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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954711Generated: October 26, 2026

Cyclohexylamine → 4-Cyclohexylamino-1-methyl imidazo [1,2-a]quinoxaline

https://huagongshe.com/reaction/1954711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant1-methylimidazo[1,2-a]quinoxaline-4(5H)-oneHCID 10774371—
Product4-Cyclohexylamino-1-methyl imidazo [1,2-a]quinoxalineHCID 10564724—

Reaction Steps

By reaction of 1-methylimidazo[1,2-a]quinoxaline-4(5H)-one (example 2) with cyclohexylamine, according to a procedure that is similar to that followed in example 9, there is obtained 4-cyclohexylamino-1-methyl imidazo [1,2-a]quinoxaline. m.p. (DSC)=126.5° C. (onset); IR (KBr): 3345, 2938, 1546 cm-1 ; 1H-NMR (CDCl3): δ8.0 (1H,dd), 7.7 (1H,dd), 7.5÷7.1 (3H,m), 6.0 (1H,d), 4.2 (1H,m), 2.85 (3H,s), 2.3÷1.95 (4H,m), 1.95÷0.9 (6H,m); UV (EtOH): λmax =225, 243, 272, 301, 316, 329 nm. Elementary analysis for C17H20N4 (m.w.280.37): calcd. C 72.83, H 7.19, N 19.98%; found C 72.21, H 7.54, N 20.14%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124287
Source datasetuspto-grants-2000_09
ORD IDord-c99f0564b71a47fbb32187705e871b36
Source noteuspto-grants-2000_09