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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785331Generated: October 28, 2026

Thionyl Chloride → HCID 57593710, compound

https://huagongshe.com/reaction/1785331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-(Methanesulfonyl)-3-nitrobenzoic acidHCID 2723871—
ReactantN2-(4-Amino-phenyl)-5-bromo-N4-[2-(3H-imidazol-4-yl)ethyl]pyrimidine-2,4-diamineHCID 57593472—
SolventDimethylacetamideHCID 31374—
ProductHCID 57593710HCID 5759371023.7%

Reaction Steps

4-Methanesulfonyl-3-nitro-benzoic acid (72 mg, 0.29 mmole) was dissolved in DMA (3 ml) and thionyl chloride (0.29 mmole) was added at ambient temperature. After the mixture was stirred for 5 minutes N2-(4-Amino-phenyl)-5-bromo-N4-[2-(3H-imidazol-4-yl)-ethyl]-pyrimidine-2,4-diamine (100 mg, 0.26 mmole, prepared according to procedure 21) was added and the reaction was allowed to stir overnight. After extraction with bicarbonate solution and ethyl acetate (3×) the combined organic layers were dried over magnesium sulfate and the solvent was removed under reduced pressure. The crude product was purified by flashmaster chromatography on silica gel to provide 37 mg of N-(4-{5-Bromo-4-[2-(3H-imidazol-4-yl)-ethylamino]-pyrimidin-2-ylamino}-phenyl}-4-methanesulfonyl-3-nitro-benzamide (23% yield). ESI-MS: 602.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504410B2
Source datasetuspto-grants-2009_03
ORD IDord-7374dfe2c0c34fff95de0663074bc577
Source noteuspto-grants-2009_03