戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1166作成日:2026年10月25日

2,4-Diamino-6-chloropyrimidine → 6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1166

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Diamino-6-chloropyrimidineHCID 67432—
反応物Sodium AcetateHCID 517045—
反応物Benzenediazonium, 4-chloro-, chlorideHCID 11819533—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamineHCID 26776441.4%

反応手順

To a suspension of 4-chloro-2,6-diaminopyrimidine (21.68 g, 0.150 mol) in water (750 ml) and acetic acid (750 ml) was added sodium acetate (300 g). Solution occurred after stirring for 20 minutes, and then the solution of 4-chlorobenzenediazonium chloride (0.166 mol) was added with cooling over 30 minutes at a rate that kept the reaction at 18°. The reaction was stirred overnight at room temperature, and the orange crystals were filtered, washed with water (4×400 ml), and dried in vacuo to give 17.6 g of 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine. The mother liquors were cooled to 5° for 20 hours, and the crystals were collected and dried in vacuo to give 6.94 g of additional 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidineadiamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723609
出典データセットuspto-grants-1998_03
ORD IDord-db70288e9ca54cb89358931186bc5974
出典メモuspto-grants-1998_03