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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535456Generated: October 30, 2026

Hydrochloric Acid → 2-Amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoic acid

https://huagongshe.com/reaction/535456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoateHCID 57500395—
SolventMethanolHCID 887—
Product2-Amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoic acidHCID 6665317388.6%

Reaction Steps

4.92 ml (4.92 mmol) of a 1N aqueous solution of sodium hydroxide are added, at ambient temperature, to 1.91 g (4.69 mmol) of methyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoate in 30 ml of methanol. The reaction medium is refluxed for 10 hours and then hydrolysed with a 1N aqueous solution of hydrochloric acid. The aqueous phase is extracted with ethyl acetate. The organic phase obtained is washed with water, dried over sodium sulphate, filtered, and concentrated under reduced pressure. The solid obtained is rinsed with diisopropyl ether and dichloromethane, and dried under reduced pressure overnight at 50° C. 1.55 g of a yellow solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859544B2
Source datasetuspto-grants-2014_10
ORD IDord-a40eb93d44604b228e910ad53f99cc34
Source noteuspto-grants-2014_10