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HRID 604870作成日:2026年10月26日

Phosgene → [5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine

https://huagongshe.com/reaction/604870

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物DiisopropylethylamineHCID 81531—
反応物3-Chloro-4-(3-chlorophenyl)-2-butanoneHCID 4250985—
反応物4-(1,2,4-Triazol-1-yl)phenylthioureaHCID 5260678—
溶媒EthanolHCID 702—
生成物[5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amineHCID 25106457—

反応条件

温度170 °C

反応手順

A suspension of 55 mg (0.25 mmol) 4-(1,2,4-triazol-1-yl)phenylthiourea, of 60 mg (0.28 mmol) 3-chloro-4-(3-chlorophenyl)-2-butanone and of 65 mg (0.5 mmol) N,N-diisopropyl ethyl amine in ethanol (2.5 ml) was refluxed over night. The same amount of chloro ketone was added and the reaction was heated to reflux over night. Again 1.1 equivalent of chloro ketone was added and the reaction was heated for 10 minutes in a microwave oven to 170° C. The solvent was evaporated and the residue was purified on silica gel with methylene chloride/methanol 19/1 yielding 27 mg (28%) [5-(3-chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine as a yellow solid. MS ISP (m/e): 382.1 (100) (M+H)+. 1H NMR (CDCl3, 250 MHz): δ (ppm)=8.48 (s, 1H), 8.09 (s, 1H), 7.60 (d, 2H), 7.46 (d, 2H), 7.25-7.18 (m, 3H), 7.09 (d, 1H), 3.96 (s, 2H), 2.29 (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-a3be7135f3944c2087df2195ee7e0bd6
出典メモuspto-grants-2011_03