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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532064Generated: November 1, 2026

N-bromobutanimide → HCID 135738546, compound

https://huagongshe.com/reaction/1532064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 135738567HCID 135738567—
SolventDimethylformamideHCID 6228—
ProductHCID 135738546HCID 13573854678%

Reaction Steps

A solution of N-bromosuccinimide (1.0 g, 0.0056 mol) in DMF (10 ml) was added dropwise to a stirred solution of 6-(2-ethoxyphenyl)-1-n-propyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one (Example 1; 0.84 g, 0.0028 mol) in DMF (10 ml) and the resulting red solution stirred for 20 hours. The solvent was removed by evaporation under vacuum and the residue partitioned between saturated aqueous sodium bicarbonate solution (20 ml) and ethyl acetate (20 ml). The organic phase was removed and the aqueous phase extracted with ethyl acetate (3×30 ml). The combined organic solutions were dried and the solvent removed by evaporation under vacuum to give an orange crystalline solid. Recrystallisation from ethyl acetate-hexane gave the title compound as colourless crystals (0.812 g, 78%), m.p. 172-173° C. Found: C,51.13; H,4.41; N,14.84. C16H17BrN4O2 requires C,50.94; H,4.54; N,14.85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200980B1
Source datasetuspto-grants-2001_03
ORD IDord-7c7894b237454472a2c344dafe7b1a76
Source noteuspto-grants-2001_03