Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982413Generated: October 28, 2026

Ammonia → 3-Methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxamide

https://huagongshe.com/reaction/1982413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 13220386HCID 13220386—
ReactantAcetone cardiceHCID 18522661—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxamideHCID 1322039679%

Reaction Steps

A flask fitted with a Dewar condenser containing dry ice/acetone was cooled in a dry ice/acetone bath and charged with 350 ml of anhydrous ammonia. A few crystals of hydrated ferric nitrate catalyst were added, and the cooling bath was removed. Lithium amide was then generated by the addition, over one hour, of 1.78 g (0.26 mole) of freshly cut lithium metal ribbon. After the addition of 65 ml of cold tetrahydrofuran, a solution of 16.5 g (0.060 mole) of 3-methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxylic acid ethyl ester in 75 ml of tetrahydrofuran was added over 30 minutes. The Dewar condenser was removed, and the mixture was stirred for 16 hours as the excess ammonia evaporated. The total reaction mixture was added to 600 g of ice/water, and the crude amide product was filtered and washed with water. Recrystallization from aqueous ethanol yielded 11.7 g (79% yield) of final product, mp 174°-177° C. An additional recrystallization as above yielded an analytically pure sample, mp 179°-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596814
Source datasetuspto-grants-1986_06
ORD IDord-96e9d4ee62704b68a9eb70d33c2c9981
Source noteuspto-grants-1986_06