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HRID 36306作成日:2026年10月25日

2-Fluorobenzoic acid → N-[2-[4-[[3-butyl-5-oxo-1-[5-(propanoylamino)-2-(trifluoromethyl)phenyl]-1,2,4-triazol-4-yl]methyl]-3-fluorophenyl]phenyl]sulfonyl-2-fluorobenzamide

https://huagongshe.com/reaction/36306

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluorobenzoic acidHCID 9935—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物5-n-butyl-2,4-dihydro-4-[(3-fluoro-2'-sulfamoyl-biphenyl-4-yl)methyl]-2-[5-(propionylamino)-2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 9986353—
触媒4-(Dimethylamino)pyridineHCID 14284—
生成物N-[2-[4-[[3-butyl-5-oxo-1-[5-(propanoylamino)-2-(trifluoromethyl)phenyl]-1,2,4-triazol-4-yl]methyl]-3-fluorophenyl]phenyl]sulfonyl-2-fluorobenzamideHCID 1025944793%

反応手順

Reaction of 5-n-butyl-2,4-dihydro-4-[(3-fluoro-2'-sulfamoyl-biphenyl-4-yl)methyl]-2-[5-(propionylamino)-2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one (from Step C) with 2-fluorobenzoic acid (3 equivalents), CDI (3 equiv), DBU (3 equiv), and DMAP (3 equiv) according to the method of Example 51 (as modified in Example 81) gave a a 93% yield of the title compound as a white, stiff foam, mp 119°-122° C.; homogeneous by TLC in 9:1 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 742 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05411980
出典データセットuspto-grants-1995_05
ORD IDord-0857376cb8d44a71bf1bd924fb40b46d
出典メモuspto-grants-1995_05