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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327042Generated: October 27, 2026

N-bromobutanimide → 5-(5-Bromo-2-propoxyphenyl)-1,6-dihydro-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/327042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-Methyl-5-(2-propoxyphenyl)-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-oneHCID 135738547—
SolventDimethylformamideHCID 6228—
Product5-(5-Bromo-2-propoxyphenyl)-1,6-dihydro-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-oneHCID 13615158983.6%

Reaction Steps

N-Bromosuccinimide (2.6 g, 0.016 mol) in dimethylformamide (40 ml) was added dropwise to a stirred solution of 5-(2-n-propoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]-pyrimidin-7-one (Preparation 10, 4.0 g. 0.010 mol) in dimethylformamide (40 ml) at room temperature. After 7 hours the solvent was removed by evaporation under vacuum, the residue suspended in saturated aqueous sodium carbonate solution, and the resulting solution extracted with ethyl acetate (3×50 ml). The organic extracts were combined, dried (Na2SO4) and evaporated under vacuum. Trituration of the residue with ether, followed by crystallisation from ethyl acetate-hexane, gave the title compound as white crystals (3.39 g, 68%), m.p. 117°-118° C. Found C,53.15; H, 5.03; N,13.78. C18H21BrN4O2 requires C,53.34; H,5.22; N,13.82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272147
Source datasetuspto-grants-1993_12
ORD IDord-0f1379dab4bd4c21a4f677ecde7af677
Source noteuspto-grants-1993_12