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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063977Generated: October 25, 2026

Sodium Hydroxide → Methyl 5-chloroimidazo[1,5-a]pyridine-6-carboxylate

https://huagongshe.com/reaction/2063977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58324544HCID 58324544—
ReactantHCID 178479711HCID 178479711—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-chloroimidazo[1,5-a]pyridine-6-carboxylateHCID 5832456588%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a suspension of 2-chloro-6-formylaminomethylnicotinic acid methyl ester (42.6 g, 0.19 mol) in toluene (400 mL) was added phosphorous (V) oxychloride (18.2 mL, 0.20 mol) and the reaction mixture heated at 65° C. for 1.5 hours. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (200 mL) before treating with sodium hydroxide solution (2 M) to adjust pH˜8. The layers were separated and the aqueous layer extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with brine (100 mL), dried (MgSO4) then charcoal (˜5 g) was added and the solution mixed for 5 minutes before being filtered and concentrated in vacuo to yield the title compound as a tan solid (34.4 g, 88%) 1H NMR (CDCl3, 400 MHz) 8.52 (1H, s), 7.57 (1H, s), 7.45 (1H, d, J=9.3 Hz), 7.25 (1H, d, J=9.1 Hz), 3.97 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288408B2
Source datasetuspto-grants-2012_10
ORD IDord-99dc6d7bbb9f4b84976dec47f18f1d84
Source noteuspto-grants-2012_10