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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690331Generated: October 29, 2026

Triethylamine → N-methyl-N-(1-methyl-1H-pyrrolo[2,3-b]pyridin-ylmethyl)acrylamide

https://huagongshe.com/reaction/1690331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactantmethyl({1-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl}methyl)amineHCID 22139044—
SolventDichloromethaneHCID 6344—
ProductN-methyl-N-(1-methyl-1H-pyrrolo[2,3-b]pyridin-ylmethyl)acrylamideHCID 6690535682.6%

Reaction Steps

A solution of acryloyl chloride (0.43 g, 5.58 mmole) in CH2Cl2 (10 mL) was added dropwise with stirring to a solution of 1-methyl-3-(methylaminomethyl)-1H-pyrrolo[2,3-b]pyridine (0.93 g, 5.28 mmole) and triethylamine (0.8 mL, 5.8 mmole) in CH2Cl2 (40 mL) at 0° C. under N2. The reaction was allowed to warm to RT and stir for 1 hr, then was concentrated in vacuo. The residue was dissolved in 10% NaOH and extracted with CH2Cl2 (3×20 mL). The extracts were dried (MgSO4), filtered, and concentrated. The residual oil was flash chromatographed on silica gel (5% MeOH/CH2Cl2) to give the title compound (1.0 g, 80%) as a colorless oil: MS (ES) m/e 216 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153652B2
Source datasetuspto-grants-2012_04
ORD IDord-1fab533534c74b93a8e2f2c447027c40
Source noteuspto-grants-2012_04