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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526342Generated: October 29, 2026

Methanol → Methyl 3-amino-3-(5-bromopyridin-3-yl)propanoate

https://huagongshe.com/reaction/526342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Amino-3-(5-bromopyridin-3-yl)propionic acidHCID 21256685—
ProductMethyl 3-amino-3-(5-bromopyridin-3-yl)propanoateHCID 5704543752%

Reaction Conditions

Temperature0 °C

Reaction Steps

9.54 g (38.93 mmol) 3-amino-3-(5-bromopyridin-3-yl)propionic acid were suspended in 158 ml methanol and the mixture cooled to 0° C. 4.26 ml (58.39 mmol) thionyl chloride were slowly added. The mixture was stirred at room temperature for 20 hours and concentrated. The residue was treated with saturated sodium hydrogen carbonate solution and extracted with dichloromethane. The organic part was dried with sodium sulfate and concentrated. Chromatography over silica gel (dichloromethane/ethanol 100/0-50/50) gave 5.84 g (52%) 3-amino-3-(5-bromopyridin-3-yl)-propionic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345793B2
Source datasetuspto-grants-2016_05
ORD IDord-75b1b11430954a0db9468824230629ef
Source noteuspto-grants-2016_05