Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490891Generated: October 27, 2026

N-bromobutanimide → CID 14590535

https://huagongshe.com/reaction/490891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-ethoxy-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 13072976—
SolventCarbon TetrachlorideHCID 5943—
ProductCID 14590535HCID 1459053550.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of Intermediate 35 (1.0 g, 3.8 mmol) and N-bromosuccinimide (1.49 g, 8.4 mmol) in carbon tetrachloride (35 ml) was heated at reflux for 3 hours. The reaction mixture was cooled in an ice-bath and the precipitate filtered. The filtrate was concentrated in vacuo and the residue dissolved in tetrahydrofuran (12.5 ml). Water (3.5 ml) and saturated sodium carbonate solution (3 ml) were added and the mixture stirred at 20° C. for 18 hours. The reaction was diluted with water and extracted with ethyl acetate. The combined organic phases were dried Na2SO4) and evaporated in vacuo. The residue was purified on an SPE cartridge (silica, 20 g) eluting with dichloromethane, chloroform, then chloroform:methanol (99:1, 49:1, 19:1 then 9:1). Appropriate fractions were combined and evaporated in vacuo to afford Intermediate 36 as an off-white solid (0.45 g). LCMS showed MH++236, TRET=2.46 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528148B2
Source datasetuspto-grants-2009_05
ORD IDord-0bfa5079a52f4029a6e3aa97174d01d0
Source noteuspto-grants-2009_05