Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204824Generated: October 25, 2026

Triethylamine → tert-butyl (5-bromo-3-(3-phenylisoxazol-5-yl)pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamate

https://huagongshe.com/reaction/2204824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-hydroxybenzenecarboximidoyl chlorideHCID 2756315—
Reactanttert-butyl N-(5-bromo-3-ethynylpyrazin-2-yl)-N-[(tert-butoxy)carbonyl]carbamateHCID 58070394—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (5-bromo-3-(3-phenylisoxazol-5-yl)pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamateHCID 5947236370%

Reaction Steps

Triethylamine (50.82 mg, 70.00 μL, 0.5022 mmol) was added to a solution of tert-butyl N-(5-bromo-3-ethynyl-pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamate (200 mg, 0.5022 mmol) and N-hydroxybenzimidoyl chloride (78.13 mg, 0.5022 mmol) in THF (16.00 mL) and the reaction mixture stirred at RT for 1 hour. After this time the reaction mixture was heated under reflux for 3 hours, cooled to RT and concentrated in vacuo. The residue was purified by column chromatography eluting with 10% EtOAc/Petroleum ether to give the product as a colourless oil that crystallised on standing (182 mg, 70% Yield). 1H NMR (400.0 MHz, DMSO) d 1.41 (18H, s), 7.37 (1H, s), 7.52 (3H, m), 7.90 (2H, m), 8.68 (1H, s); MS (ES+) 519.05

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365557B2
Source datasetuspto-grants-2016_06
ORD IDord-bca6829038cf4d22870c5c74b3214f41
Source noteuspto-grants-2016_06