Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399965Generated: November 4, 2026

Potassium Acetate → 2-(3-Ethylureido)-7-(pyridin-2-yl)benzothiazol-5-ylboronic acid

https://huagongshe.com/reaction/1399965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(neopentyl glycolato)diboronHCID 2734316—
ReactantHCID 72724619HCID 72724619—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-Ethylureido)-7-(pyridin-2-yl)benzothiazol-5-ylboronic acidHCID 7272448388.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of xi (25 g, 56.1 mmol) in DMSO (250 mL) at RT was added bis(neopentylglycolato)diboron (25.2 g, 112 mmol) and KOAc (16.5 g, 168 mmol). The resulting reaction mixture was de-gassed by purging N2 for 15-20 min followed by addition of Pd(dppf)Cl2 (6.8 g, 8.4 mmol). The mixture was purged with N2 for 15-20 min and then heated to 80° C. for 90 min. The reaction was poured onto saturated NH4Cl solution (1 L). The resulting precipitate was filtered and dried under vacuum. The solid cake was taken in 2M NaOH (200 mL) and stirred for 45 min at RT. The solution was filtered and the filtrate was acidified up to pH 5-6 and the resulting solid collected by filtration to give Intermediate 1 (17 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906902B2
Source datasetuspto-grants-2014_12
ORD IDord-5a93c78a0be2407e9744a7851cffbfdb
Source noteuspto-grants-2014_12