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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32542Generated: October 30, 2026

Azobisisobutyronitrile → 2-(2-Bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/32542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(1-Methyl-4-phenyl-1H-imidazol-5-yl)-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidineHCID 69194465—
SolventCarbon TetrachlorideHCID 5943—
Product2-(2-Bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidineHCID 6919448139%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2-(1-methyl-4-phenyl-1H-imidazol-5-yl)-7-(methylthio)[1,3]thiazolo-[5,4-d]pyrimidine (Intermediate 42) (0.25 g), N-bromosuccinimide (0.26 g) and AIBN (37 mg) in carbon tetrachloride (30 mL) was heated at 70° C. for 18 hours The suspension was filtered and the residue washed well with CCl4. The solvent was evaporated in vacuo to give a yellow solid. Purification by flash chromatography on silica eluting with EtOAC:hexane (1:9) gave the title compound as a white solid (0.12 g, 39%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427616B2
Source datasetuspto-grants-2008_09
ORD IDord-40c12e99f5124d6abda2d968f5823005
Source noteuspto-grants-2008_09