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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112714Generated: October 27, 2026

Triethylamine → (E)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)-3-[6-(3-methylureido)pyridin-3-yl]acrylamide

https://huagongshe.com/reaction/2112714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl IsocyanateHCID 12228—
Reactant3-(6-Aminopyridin-3-Yl)-N-Methyl-N-((1-Methyl-1h-Indol-2-Yl)Methyl)AcrylamideHCID 5287720—
SolventDimethylformamideHCID 6228—
Product(E)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)-3-[6-(3-methylureido)pyridin-3-yl]acrylamideHCID 984268643.4%

Reaction Steps

Methyl isocyanate (0.18 mL, 3.05 mmole) was added to a solution of (E)-3-(6-aminopyridin-3-yl)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamide (0.20 g, 0.61 mmole) and triethylamine (0.17 mL, 1.22 mmole) in DMF (20 mL) at RT. The reaction was stirred for 5 days, then was concentrated in vacuo, and the residue was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated. Flash chromatography on silica gel (ethyl acetate) gave the title compound (0.10 g, 43%) as an off white solid: MS (ES) m/e 378 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524843B2
Source datasetuspto-grants-2009_04
ORD IDord-30b15d74a5434881990029963170d66e
Source noteuspto-grants-2009_04