Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596076Generated: October 29, 2026

Sodium Thiosulfate → Tert-butyl 4-(2-amino-5-bromopyridin-3-yl)-2-fluorobenzoate

https://huagongshe.com/reaction/596076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-(2-aminopyridin-3-yl)-2-fluorobenzoateHCID 118045884—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(2-amino-5-bromopyridin-3-yl)-2-fluorobenzoateHCID 11804619290%

Reaction Steps

A solution of tert-butyl 4-(2-aminopyridin-3-yl)-2-fluorobenzoate (700 mg, 2.43 mmol) in acetonitrile (10 mL) was treated with NBS (453 mg, 2.55 mmol). After 10 min, the reaction was completed. The reaction was treated with 1:1 sat. aq. NaHCO3: sat.aq. Na2S2O3 (10 mL). The mixture was stirred vigorously for 10 min. The mixture was diluted with ethyl acetate (30 mL) and the layers were separated. The organics were washed with brine, dried over magnesium sulfate, filtered and concentrated to provide tert-butyl 4-(2-amino-5-bromopyridin-3-yl)-2-fluorobenzoate (803 mg, 90% yield). LCMS (m/z): 367.2, 369.2 (MH+), 0.75 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-e66cffe4a97b474d855455a16bed46c4
Source noteuspto-grants-2016_01