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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183551Generated: October 27, 2026

Methyl acetoacetate → 7-amino-1,5-dimethyl-3-(2,4,6-trimethyl-phenyl)-1H-pyrrolo[3,2-b]pyridine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/2183551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantTin tetrachlorideHCID 24287—
Reactant3-amino-1-methyl-4-(2,4,6-trimethylphenyl)-1H-pyrrole-2-carbonitrileHCID 22474443—
Solvent1,2-DichloroethaneHCID 11—
Product7-amino-1,5-dimethyl-3-(2,4,6-trimethyl-phenyl)-1H-pyrrolo[3,2-b]pyridine-6-carboxylic acid methyl esterHCID 54043777—

Reaction Steps

A mixture of 3-amino-1-methyl-4-(2,4,6-trimethylphenyl)-1H-pyrrole-2-carbonitrile (2 mmol), methyl acetoacetate (4 mmol) and SnCl4 (4 mmol) in 1,2-dichloroethane was heated at reflux for about six hours until all the starting material were consumed. The mixture was quenched with acetone, basified with saturated NaHCO3, then filtered through Celite?. The filtrate was concentrated to dryness. The residue was quenched with water and extracted with chloroform. The chloroform layer was washed with brine, dried and concentrated to dryness to give 7-amino-1,5-dimethyl-3-(2,4,6-trimethyl-phenyl)-1H-pyrrolo[3,2-b]pyridine-6-carboxylic acid methyl ester. The product may be purified by trituration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900217B2
Source datasetuspto-grants-2005_05
ORD IDord-3eaa85f08312493d9154aff17c0376f7
Source noteuspto-grants-2005_05