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HRID 237作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonamide, 3-amino-HCID 7377—
反応物2,4-DichloropyrimidineHCID 77531—
試薬Cesium carbonateHCID 10796—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Palladium (II) acetateHCID 4144353—
溶媒1,4-DioxaneHCID 31275—
生成物3-[(4-Chloropyrimidin-2-yl)amino]benzenesulfonamideHCID 889048942%

反応条件

温度150 °C

反応手順

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.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-07751cbdbcad4c89bdfeeea3a04ddb39
出典メモ750 AstraZeneca ELN dataset