戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 59463作成日:2026年10月24日

1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)- → 4-(3-(2-Chloro-6-fluorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-2-methoxy-N-(5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)benzamide

https://huagongshe.com/ja/reaction/59463

反応式

関与物質

役割名称HCID仕込み量
反応物1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-HCID 82634—
反応物TrimethylaluminumHCID 16682925—
反応物methyl 4-(3-(2-chloro-6-fluorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-2-methoxybenzoateHCID 136492448—
溶媒TolueneHCID 1140—
生成物4-(3-(2-Chloro-6-fluorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-2-methoxy-N-(5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)benzamideHCID 13661252418.7%

反応手順

The title compound was prepared by following the procedure as described for Example-31 by using methyl 4-(3-(2-chloro-6-fluorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-2-methoxybenzoate (step-2 of Intermediate-15, 0.100 g, 0.26 mmol), 5-(trifluoromethyl)-1,3,4-thiadiazol-2-amine (0.059 g, 0.34 mmol), trimethyl aluminium (2M solution in toluene) (0.5 mL) and dry toluene (5.0 mL) to afford 0.025 g of desired product. 1H NMR (DMSO-d6): δ 3.95 (s, 3H), 7.51 (t, J=9.0 Hz, 1H), 7.87-7.76 (m, 3H), 7.78 (s, 1H), 7.85 (d, J=8.7 Hz, 1H), 12.86 (br s, 2H); MS (m/z): 514.90 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09439890B2
出典データセットuspto-grants-2016_09
ORD IDord-547dbe2b0c1d40e3bace9a2df7b61c0e
出典メモuspto-grants-2016_09