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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007083Generated: October 30, 2026

1,2-Dimethoxyethane → Ethyl 3-[2-(tert-butoxycarbonylaminomethyl)phenyl]pyridine-2-carboxylate

https://huagongshe.com/reaction/1007083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(2-(((tert-Butoxycarbonyl)amino)methyl)phenyl)boronic acidHCID 10911965—
ReactantEthyl 3-bromopyridine-2-carboxylateHCID 15141568—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-[2-(tert-butoxycarbonylaminomethyl)phenyl]pyridine-2-carboxylateHCID 1201723266%

Reaction Steps

150 ml of 1,2-dimethoxyethane were aerated with argon, and 874 mg (0.75 mmol) of Pd(PPh3)4 and 3.45 g (15 mmol) ethyl 3-bromopyridine-2-carboxylate were added. After 10 min, 5.53 g (22.5 mmol) of 2-(tert-butoxycarbonylaminomethyl)phenylboronic acid and finally 15 ml of a 2M sodium carbonate solution were added. The mixture was heated to reflux for 18 h under argon, diluted with dichloromethane after cooling and washed with water. The organic phase was dried, concentrated and purified by chromatography on silica gel. 3.4 g (66%) of a viscous oil were obtained. MS (ES+): m/z=357 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794377B2
Source datasetuspto-grants-2004_09
ORD IDord-a8c4c6cec10544fdbebc3bcc59a94df2
Source noteuspto-grants-2004_09