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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112250Generated: November 3, 2026

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

https://huagongshe.com/reaction/1112250

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 15 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 numberUS04120962
Source datasetuspto-grants-1978_10
ORD IDord-455ac48a69f846bb9b8c7923f3c01420
Source noteuspto-grants-1978_10