Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420520Generated: October 30, 2026

Chloroacetaldehyde → Methyl 6-bromoimidazo[1,2-a]pyridine-7-carboxylate

https://huagongshe.com/reaction/420520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-amino-5-bromoisonicotinateHCID 25307230—
SolventEthanolHCID 702—
ProductMethyl 6-bromoimidazo[1,2-a]pyridine-7-carboxylateHCID 5790657691.7%

Reaction Steps

A mixture of 2-amino-5-bromo-isonicotinic acid methyl ester (500 mg, 2.16 mmol), NaHCO3 (309 mg, 3.68 mmol) and chloracetaldehyde (1.16 mL, 9.8 mmol) in EtOH (15 mL) was vigorously stirred and refluxed for 14 h. The reaction mixture was cooled to RT, concentrated under vacuum and the remaining residue was suspended in AcOEt (100 mL). The organic fraction was washed with water (2×50 mL), then dried over Na2SO4, filtered, and evaporated. The residue was purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; gradient elution, [hexane/DCM 1:1]/TBME 95:5-100% TBME) to yield the title compound (505 mg, 1.98 mmol, 91%). MS: 255 [M+1]+; HPLC: AtRet=0.58 TLC: RF 0.16 (hexane/DCM/TBME 1:1:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097617B2
Source datasetuspto-grants-2012_01
ORD IDord-094f558165b94efeadd276b2003c215a
Source noteuspto-grants-2012_01