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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908483Generated: November 1, 2026

N-bromobutanimide → HCID 67388478, compound

https://huagongshe.com/reaction/908483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67388437HCID 67388437—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67388478HCID 6738847888.9%

Reaction Steps

A mixture of 1-bromopyrrolidine-2,5-dione (44.5 mg) and 2-(2-amino-3-pyridyl)-1,3-benzoxazole-7-carbonitrile (59 mg) in tetrahydrofuran (5 ml) was stirred at room temperature for 1 hour. The reaction was incomplete and further 1-bromopyrrolidine-2,5-dione (44.5 mg) was added at room temperature and the reaction mixture was stirred at room temperature for 1 hour. The resulting precipitate was collected by filtration, washed with acetonitrile (2×2 ml) and dried to a constant weight to afford 2-(2-amino-5-bromo-3-pyridyl)-1,3-benzoxazole-7-carbonitrile (70.0 mg) as a pale brown solid. NMR Spectrum: (DMSOd6) 7.61 (dd, 1H), 7.85 (bs, 2H), 7.96 (dd, 1H), 8.20 (dd, 1H), 8.37 (d, 1H), 8.39 (d, 1H); Mass spectrum: M(+CH3CN)+H+ 356-358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017611B2
Source datasetuspto-grants-2011_09
ORD IDord-5ed09b9b8e0a4969bf83dc8f070b43a4
Source noteuspto-grants-2011_09