戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 76530作成日:2026年10月23日

4-Nitro-1,3-benzenediamine → N2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/ja/reaction/76530

反応式

関与物質

役割名称HCID仕込み量
反応物4-Nitro-1,3-benzenediamineHCID 21208—
反応物2,4-Dichloro-5-fluoropyrimidineHCID 250705—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物N2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamineHCID 22060904—

反応条件

温度70 °C

反応手順

2,4-Dichloro-5-fluoropyrimidine (50 mg, 0.3 mmol) was dissolved in a mixture of MeOH (1 ml) and H2O (0.1 ml). 3-amino-4-nitroaniline (184 mg, 1.2 mmol) was added and the mixture was refluxed for 3 days (70° C. oil-bath temperature). The mixture was cooled to 22° C., concentrated to dryness under reduced pressure and subjected to column chromatography on silica gel (CHCl3-Acetone, 2:1) to give N2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (DMSO-d6+CD3OD): δ 8.21 (d, 1H, J=2.9 Hz), 7.89 (m, 3H), 7.56 (d, 1H, J=2.3 Hz), 7.01 (m, 1H), 6.81 (dd, 1H, J=2.3, 9.4 Hz); LCMS: purity: 91.1%; MS (m/e): 401.00 (M+, 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835430B2
出典データセットuspto-grants-2014_09
ORD IDord-0f06a554a588467391aaf4cce9952431
出典メモuspto-grants-2014_09