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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362328Generated: October 31, 2026

N-bromobutanimide → HCID 67960573, compound

https://huagongshe.com/reaction/2362328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67960315HCID 67960315—
SolventAcetonitrileHCID 6342—
ProductHCID 67960573HCID 67960573—

Reaction Steps

To 5-((4-methylquinazolin-2-yl)methyl)-7,8-dihydro-3H-imidazo[2,1-b]purin-4(5H)-one 13 (386 mg, 1.16 mmol) in CH3CN (10 ml) was added NBS (268 mg, 1.51 mmol) at 0° C., stirred for 1.5 hr. Another 41 mg of NBS was added, stirred for 30 minutes. The reaction was quenched by adding water (15 ml), washed with DCM (2×15 ml). The organic phase was washed with HCl (1 M, 10 ml). The combined aqueous phase was concentrated and purified by flash chromatography (MeOHIDCM, MeOH contains 1% Et3N) to afford 2-bromo-5-((4-methylquinazolin-2-yl)methyl)-7,8-dihydro-3H-imidazo[2,1-b]purin-4(5H)-one 14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691832B2
Source datasetuspto-grants-2014_04
ORD IDord-160b236dd91d4e95b5db5af6ef0f5538
Source noteuspto-grants-2014_04