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HRID 226597作成日:2026年10月24日

Hydrochloric Acid → 2-chloro-5-fluoro-N4-(3-methyloxycarbonyl-4-methoxyphenyl)-4-pyrimidineamine

https://huagongshe.com/ja/reaction/226597

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物NitrogenHCID 947—
反応物Methyl 5-amino-o-anisateHCID 89843—
反応物2,4-Dichloro-5-fluoropyrimidineHCID 250705—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2-chloro-5-fluoro-N4-(3-methyloxycarbonyl-4-methoxyphenyl)-4-pyrimidineamineHCID 22060802—

反応条件

温度60 °C

反応手順

The reaction flask equipped with a magnetic stirring bar and a rubber septum (to prevent loss of 2,4-dichloro-5-fluoropyrimidine and N2 inlet was charged with 3-methyloxycarbonyl-4-methoxyaniline (0.88 g, 4.86 mmol), MeOH (3 mL), H2O (7 mL) and 2,4-dichloro-5-fluoropyrimidine (0.81 g, 4.86 mmol). The reaction mixture was stirred at 60° C. for 30 min., diluted with H2O (50 mL), acidified with 2N HCl (6 mL) and sonicated. The solid obtained was filtered, washed with H2O and dried to produce 2-chloro-5-fluoro-N4-(3-methyloxycarbonyl-4-methoxyphenyl)-4-pyrimidineamine R940302. 1H NMR (DMSO-d6): δ 10.10 (1H, s), 8.39 (1H, d, J=3.6 Hz), 8.04 (1H, d, J=2.7 Hz), 7.98–7.93 (1H, m), 7.30 (1H, d, J=9 Hz), 3.92 (3H, s), 3.89 (3H, m); purity 96%; MS (m/e): 312 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557210B2
出典データセットuspto-grants-2009_07
ORD IDord-e892d3242dce45148960ea527fcb8ab1
出典メモuspto-grants-2009_07