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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565036Generated: October 31, 2026

Ammonium formate → Ethyl 7-[(3-aminopropyl)amino]-1-methyl-2-indolecarboxylate

https://huagongshe.com/reaction/565036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantBenzyl (3-Oxopropyl)carbamateHCID 10398106—
ReactantAzane;hydrateHCID 12896473—
ReactantEthyl 7-amino-1-methyl-2-indolecarboxylateHCID 21194578—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductEthyl 7-[(3-aminopropyl)amino]-1-methyl-2-indolecarboxylateHCID 2119403624.6%

Reaction Steps

A mixture of 4.00 g (18.3 mmol) of ethyl 7-amino-1-methyl-2-indolecarboxylate, 7.60 g (37.6 mmol) of 3-(benzyloxycarbonylamino)propion aldehyde, 2.43 g (38.6 mmol) of sodium cyanoborohydride, 2.1 ml of acetic acid, 5.0 g of molecular sieves 3A and 200 ml of methanol was stirred at room temperature for 4.5 hours. After 28% ammonia water was added to the reaction solution to render the system alkaline, the reaction mixture was extracted three times with ethyl acetate. The combined extracts were then washed with saturated sodium chloride aqueous solution. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was suspended in 100 ml of ethanol. After 6.40 g (101 mmol) of ammonium formate and 0.91 g of 10% palladium/carbon were added to the suspension, the mixture was heated to reflux for 8 hours. Insoluble matters were filtered off and the filtrate was concentrated under reduced pressure. The thus obtained residue was isolated and purified by silica gel column chromatography to give 1.04 g (24.6%) of ethyl 7-[(3-aminopropyl)amino]-1-methyl-2-indolecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-7c77ef8b4449432ea37dba84c3a6a1a8
Source noteuspto-grants-2001_01