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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163585Generated: November 2, 2026

Cyanoacetamide → 6-Amino[1,3]dioxolo[4,5-g]quinoline-7-carboxamide

https://huagongshe.com/reaction/2163585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
Reactant6-Amino-1,3-benzodioxole-5-carbaldehydeHCID 290836—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product6-Amino[1,3]dioxolo[4,5-g]quinoline-7-carboxamideHCID 531189989.3%

Reaction Steps

To sodium methoxide (1.90 g., 0.03 mole) in methanol (50 ml.) is added 4,5-methylenedioxy-2-aminobenzaldehyde (5.0 g., 0.03 mole) and 2-cyanoacetamide (2.50 g., 0.03 mole). The mixture is heated to reflux for fifteen minutes and then cooled in an ice bath. The bright yellow solid is filtered off and recrystallized from acetic acid to give 6.18 g. (89.3%) of the desired product. M.P. 308° C. (dec.). (m/e = 231)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134981
Source datasetuspto-grants-1979_01
ORD IDord-59c2765fb41d47668bc0815c51f50732
Source noteuspto-grants-1979_01