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HRID 36287作成日:2026年10月26日

2-Chlorobenzoic Acid → 5-n-Butyl-2-[5-(N-n-butylcarbamoyl)-2-chlorophenyl]-4-[[2'-[N-(2-chlorobenzoyl)sulfamoyl]-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/36287

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chlorobenzoic AcidHCID 8374—
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-[5-(N-n-butylcarbamoyl)-2-chlorophenyl]-4-[(3-fluoro-2'-sulfamoylbiphenyl-4-yl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 10371596—
溶媒Diethyl EtherHCID 3283—
生成物5-n-Butyl-2-[5-(N-n-butylcarbamoyl)-2-chlorophenyl]-4-[[2'-[N-(2-chlorobenzoyl)sulfamoyl]-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1010160842%

反応手順

By the procedure of Example 51, 5-n-butyl-2-[5-(N-n-butylcarbamoyl)-2-chlorophenyl]-4-[(3-fluoro-2'-sulfamoylbiphenyl-4-yl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one (from Step G) was reacted with 2-chlorobenzoic acid (2 equivalents), CDI (2 equiv), and DBU (2 equiv). Flash chromatography of the crude product on silica gel (gradient elution with 0.5-5% MeOH in CH2Cl2) followed by trituration with ether afforded a 42% yield of the title compound as a white solid, mp 218°-220° C.; homogeneous by TLC (95:5 CH2Cl2 --MeOH); mass spectrum (FAB) m/e 753 (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-9819b0da9e9549ddbe6cb0af258ed363
出典メモuspto-grants-1995_05