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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32543Generated: October 25, 2026

2-(2-Bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amine → 2-(2-Methoxy-1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amine

https://huagongshe.com/reaction/32543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amineHCID 10068778—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product2-(2-Methoxy-1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amineHCID 1033720778%

Reaction Steps

Sodium methoxide (31 mg) was added to a solution of 2-(2-bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amine (Example 26) (22 mg) in MeOH (1 mL). The reaction was stirred and refluxed for 4 days with further sodium methoxide (31 mg) added each day. The solvent was evaporated in vacuo and water (5 mL) added. Extracted with DCM (2×5 mL) and the combined organics were dried over MgSO4, filtered and the solvent evaporated in vacuo to give a white solid (15 mg, 78%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427616B2
Source datasetuspto-grants-2008_09
ORD IDord-d63a9f812b82417f887e6e325571bd54
Source noteuspto-grants-2008_09