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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368556Generated: October 30, 2026

N-bromobutanimide → HCID 25061712, compound

https://huagongshe.com/reaction/2368556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57600225HCID 57600225—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25061712HCID 2506171231%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-methyl-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one (1.0 g, 3.8 mmol) in THF (50 mL) was added N-bromosuccinimide (0.75 g, 4.2 mol). The mixture was heated at 70° C. for 1 h and concentrated in vacuum. The residue was taken up in water and EtOAc. The organic layer was separated and the aqueous layer was extracted with ethyl acetate three times. The combined organic layers were dried (MgSO4), filtered, and concentrated in vacuum. The residue was purified by preparative LCMS to provide the desired product as a white powder (0.4 g, 30% yield). 1HNMR (400 MHz, d6-DMSO): δ 4.18 (t, J=7.5 Hz, 2H), 2.71 (s, 3H), 1.79 (m, 2H), 1.29 (m, 4H), 0.84 (m, 3H). LCMS calculated for C12H16BrN6O (M+H): 339.1, 341.1. Found: 339.1, 341.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703783B2
Source datasetuspto-grants-2014_04
ORD IDord-c8ff4f8d01624c099c841d844109c2b2
Source noteuspto-grants-2014_04