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HRID 604865作成日:2026年10月26日

3-Chloro-4-(4-chlorophenyl)-2-butanone → [5-(4-Chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

https://huagongshe.com/reaction/604865

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-(4-chlorophenyl)-2-butanoneHCID 4054027—
反応物[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
生成物[5-(4-Chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amineHCID 25107256—

反応手順

The title compound was prepared in analogy to example 1 step e) from 72 mg (0.33 mmol) 3-chloro-4-(4-chlorophenyl)-2-butanone and 79 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea. The crude product was purified on silica gel with methylene chloride/methanol 9/1 yielding 78 mg (61%) [5-(4-chloro-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a light brown solid. MS ISP (m/e): 425.1/427.1 (100/42) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.15 (s, 1H), 7.64 (s, 1H), 7.52 (s, 1H), 7.37 (d, 2H), 7.26 (d, 2H), 7.23 (s, 2H), 3.98 (s, 2H), 3.77 (s, 3H), 2.23 (s, 3H), 2.14 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910740B2
出典データセットuspto-grants-2011_03
ORD IDord-0e999940f615462cb06b37029afe7714
出典メモuspto-grants-2011_03