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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024612Generated: November 1, 2026

Dimethylformamide → HCID 57899369, compound

https://huagongshe.com/reaction/1024612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantHCID 57899416HCID 57899416—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
ProductHCID 57899369HCID 57899369—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-{5-(4-chloro-phenyl)-4-oxo-6-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-4,5-dihydro-pyrazolo[3,4-d]pyrimidin-1-yl}-benzene sulfonamide (0.300 g, 0.496 mmol) in N,N-dimethylformamide (25 mL) is degassed with argon for 0.5 h. Then 2-amino-5-bromopyridine (0.128 g, 0.745 mmol), cesium carbonate (0.323 g, 0.993 mmol), Pd(dppf)2Cl2 (0.036 g, 0.049 mmol) is added and the resulted mixture is degassed with argon for 0.5 h. The reaction mixture is then heated at 100° C. for 4 h. The reaction mixture is cooled to rt and diluted with water and extracted with ethyl acetate (3×). The combined organic layer is washed with brine, dried over Na2SO4, concentrated, and purified by preparative HPLC to afford 3-[2-[4-(6-amino-pyridin-3-yl)-phenyl]-1-(4-chloro-phenyl)-6-oxo-1,6-dihydro-purin-9-yl]-benzene sulfonamide. 1H NMR (DMSO-d6, 400 MHz) δ 8.66 (s, 1H), 8.23 (s, 1H), 8.07 (m, 1H), 7.94 (m, 1H), 7.83 (m, 1H), 7.67 (m, 1H), 7.58 (m, 2H), 7.35-7.48 (m, 10H), 6.47 (d, 1H), 6.15 (br, 1H); LC-MS calculated for C28H20ClN7O3S (M+H+) 570.1, found 570.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722691B2
Source datasetuspto-grants-2014_05
ORD IDord-d133dcc7684d46979dfcbd7cf043f3b7
Source noteuspto-grants-2014_05