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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29509Generated: October 25, 2026

1-Methylimidazole → (2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanone

https://huagongshe.com/reaction/29509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
Reactant2-Amino-5-chlorobenzoic acidHCID 12476—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product(2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanoneHCID 1099897713.7%

Reaction Steps

To a solution of nBuLi (0.0730 mol) in hexane was added N-methyl imidazole (0.0608 mol) drop wise at -40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 3 hr at rt, and then refluxed for 1 h. 2-amino-5-chlorobenzoic acid (1.74 g, 0.01014 mole) in dry ether (60 ml) was then added to the reaction mixture. The reaction mixture was stirred overnight at rt. To the reaction mixture was added saturated NH4Cl solution and the resulting mixture extracted with ethyl acetate (2×150 ml). The combined organic layers were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 300 mg (13.7%) of product as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420055B2
Source datasetuspto-grants-2008_09
ORD IDord-435f973cdb9d4431b3d43eeefb9a3641
Source noteuspto-grants-2008_09