Brief introduction of N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide

262368-30-9 N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide 21927707, apiperazines compound, is more and more widely used in various fields.

262368-30-9, N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide is a piperazines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

The 2L glass reaction flask was 900 ml purged of unitz methanol, 90.0g 1 – acetyl -3 – [methoxy (phenyl) methylene] -2 – oxodihydroindole -6 – methyl formate (compound A) and 80.6g compound N – (4 – aminophenyl) – N, respectively. 4 -Dimethyl -1 18.2g – piperazine acetamide 45 – 50 C (25 – 30 C Compound 3h B), heating and 45 – 50 C temperature-2h raising to 1h 10:1 Drying, yield (3Z) -3 – {[ (4 – {methyl – [(4 – methylpiperaz -1 – yl) acetyl] amino} phenyl} amino} – (phenyl) methylene} -2 – oxo -2, 3 -dihydroindole -6 – methyl formate (compound C) 126.3g, CFC-91.37%,99.89%., 262368-30-9

262368-30-9 N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide 21927707, apiperazines compound, is more and more widely used in various fields.

Reference:
Patent; Shiyao Group Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd.; Shiyao Group Enbipu Pharmaceutical Co., Ltd.; Wu Lihong; Liang Min; Zhong Wenhui; Zhang Sujuan; Li Dongmei; Wang Yue; Sun Wentao; Chi Xiaolei; (10 pag.)CN109988094; (2019); A;,
Piperazine – Wikipedia
Piperazines – an overview | ScienceDirect Topics