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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562104Generated: October 28, 2026

N-Methylethylamine → 5-(5-{[ethyl(methyl)amino]methyl}-3-thienyl)-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylethylamineHCID 12219—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-formyl-3-thienyl)-1H-indole-7-carboxamideHCID 57732703—
CatalystAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
Product5-(5-{[ethyl(methyl)amino]methyl}-3-thienyl)-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamideHCID 1603748061.4%

Reaction Steps

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-formyl-3-thienyl)-1H-indole-7-carboxamide (50 mg, 0.11 mmol) in DMSO (2.0 mL) was added 2 drops of acetic acid, ethyl(methyl)amine (59 mg, 1.0 mmol), and stirred at room temperature for 5 h. To this was then added sodium triacetoxyborohydride (212 mg, 1.0 mmol) and reacted overnight. It was then purified by Gilson Preparatory HPLC to give 30.0 mg of the title compound (61.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063071B2
Source datasetuspto-grants-2011_11
ORD IDord-269d1644a43042c394c3778c81f9a0c5
Source noteuspto-grants-2011_11