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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736343Generated: October 29, 2026

2-Fluorobenzenesulphonyl chloride → N-[6-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-2-yl]-2-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/736343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzenesulphonyl chlorideHCID 137761—
Reactant(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-(6-amino-pyridin-2-yl)-methanoneHCID 68908256—
SolventPyridineHCID 1049—
ProductN-[6-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-2-yl]-2-fluoro-benzenesulfonamideHCID 6890471940%

Reaction Conditions

Temperature40 °C

Reaction Steps

2-Fluoro-benzenesulfonyl chloride (72 mg, 0.37 mmol) was added to a solution of (4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-(6-amino-pyridin-2-yl)-methanone (100 mg 0.34 mmol) in pyridine (2 mL). The resulting solution was heated to 40° C. in a sealed tube for 12 h. The reaction mixture was concentrated in vacuo and the residue was triturated with MeOH and filtered to provide a crude yellow solid. Purification by flash column chromatography (hexanes/ethyl acetate 5:5-1:9) afforded the title compound as a yellow solid (60 mg, 40%). MS: 455.1 (MH+); HPLC Rf: 4.67 min. (HPLC method 4); HPLC purity: 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595325B2
Source datasetuspto-grants-2009_09
ORD IDord-ea57494840024654aacebb9a7711a48a
Source noteuspto-grants-2009_09