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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21590Generated: October 27, 2026

Ammonia → 5-Methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/21590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantLithium amideHCID 24532—
ReactantLithiumHCID 3028194—
Reactantmethyl 5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxylateHCID 13840803—
SolventTetrahydrofuranHCID 8028—
Product5-Methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamideHCID 1075306376%

Reaction Steps

Lithium amide in liquid ammonia is prepared as described by Unangst PC and Carethers ME, J. Heterocyclic Chem. 1984;21:709, from lithium metal ribbon (0.059 g, 8.5 mmol). A solution of methyl 5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxylate (0.15 g, 0.57 mmol; Unangst PC, et al., J, Heterocyclic Chem. 1987;24:811) in 4.0 mL of tetrahydrofuran is added dropwise. The mixture is stirred for 1 hour and the excess ammonia is allowed to evaporate. The residue is diluted with ethyl acetate, and the organic layer is washed with 1.0N HCl brine, saturated sodium bicarbonate solution, and brine again. The solution is dried (anhydrous magnesium sulfate) and evaporated. Recrystallization of the residue from ethyl acetatehexane gives 0.11 g (76%) of product; mp 138.5°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424329
Source datasetuspto-grants-1995_06
ORD IDord-0e93488b29b740aba879b81f4633c0a3
Source noteuspto-grants-1995_06