Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237Generated: October 23, 2026

Benzenesulfonamide, 3-amino- → 3-[(4-Chloropyrimidin-2-yl)amino]benzenesulfonamide

https://huagongshe.com/en/reaction/237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, 3-amino-HCID 7377—
Reactant2,4-DichloropyrimidineHCID 77531—
ReagentCesium carbonateHCID 10796—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,4-DioxaneHCID 31275—
Product3-[(4-Chloropyrimidin-2-yl)amino]benzenesulfonamideHCID 889048942%

Reaction Conditions

Temperature150 °C

Reaction Steps

2,4-dichloropyrimidine (200 mg, 1.34 mmol), 3-aminobenzenesulfonamide (231 mg, 1.34 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (93 mg, 0.16 mmol), cesium carbonate (875 mg, 2.68 mmol) and diacetoxypalladium (15.07 mg, 0.07 mmol) were suspended in dioxane (5 mL) and sealed into a microwave tube. The reaction was heated to 150 °C for 30 minutes in the microwave reactor and cooled to RT. The reaction mixture was diluted with EtOAc (150 mL) and washed with water (150 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 4% (10:1 MeOH/NH3 (aq)) in DCM. NMR analysis showed a trace amount of product.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-07751cbdbcad4c89bdfeeea3a04ddb39
Source note750 AstraZeneca ELN dataset