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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852599Generated: October 27, 2026

Hydrochloric Acid → methyl 4-amino-1-ethyl-1H-indole-6-carboxylate hydrochloride

https://huagongshe.com/reaction/852599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-amino-1H-indole-6-carboxylateHCID 14243967—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Productmethyl 4-amino-1-ethyl-1H-indole-6-carboxylate hydrochlorideHCID 6935967466%

Reaction Steps

To a solution of methyl 4-amino-1H-indole-6-carboxylate (D201) (900 mg, 4,74 mmol, 1 equiv) in DMF (25 ml) at room temperature was added NaH (60% dispersion in mineral oil, 200 mg, 5 mmol, 1.05 equiv) and after 15 min ethyl iodide (400 μl, 5 mmol, 1.05 equiv). The resulting mixture was stirred for 30 min then most of the solvent was removed in vacuo. The residue was diluted with AcOEt and the organic phase was washed with a 2N aqueous HCl solution, dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (iso-hexane/AcOEt: 1/1) gave an oil which was diluted with Et2O and treated with a 4N HCl solution in Et2O. The precipitate obtained was filtrated off to give methyl 4-amino-1-ethyl-1H-indole-6-carboxylate hydrochloride salt (D202) (800 mg, 66%) as a white solid. [M+H]+=219.0, RT=2.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-73f3cfe52d974fcaa601b80632df6784
Source noteuspto-grants-2007_08