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HRID 36255作成日:2026年10月23日

Propyl isocyanate → 4''-{3-Butyl-1-[2-chloro-5-(3-propyl-ureido)-phenyl]-5-oxo-1,5-dihydro-[1,2,4]triazol-4-ylmethyl}-biphenyl-2-sulfonic acid 2-chloro-benzoylamide

https://huagongshe.com/ja/reaction/36255

反応式

関与物質

役割名称HCID仕込み量
反応物Propyl isocyanateHCID 61033—
反応物4''-[1-(5-Amino-2-chloro-phenyl)-3-butyl-5-oxo-1,5-dihydro-[1,2,4]triazol-4-ylmethyl]-biphenyl-2-sulfonic acid 2-chloro-benzoylamideHCID 10032193—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
生成物4''-{3-Butyl-1-[2-chloro-5-(3-propyl-ureido)-phenyl]-5-oxo-1,5-dihydro-[1,2,4]triazol-4-ylmethyl}-biphenyl-2-sulfonic acid 2-chloro-benzoylamideHCID 1025941161%

反応手順

At room temperature, under N2, a solution of 34 mg (0.052 mmole) of 2-(5-amino-2-chlorophenyl)-5-n-butyl-4-[[2'-[N-(2-chlorobenzoyl)sulfamoyl]biphenyl-4-yl]methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one (from Example 60), 6.4 mg (0.052 mmole) of DMAP, 23 mg (0.26 mmole) of propyl isocyanate, and 1 mL of pyridine was stirred overnight. After quenching with water, the organic material was extracted with EtOAc, washed with water and brine, and dried over sodium sulfate. The crude product obtained after filtration and removal of volatiles was flash chromatographed over silica gel (gradient elution with 0.5-5% MeOH/CH2Cl2) to give 23 mg (61%) of the desired compound as a white solid, mp >208° C. (gradual), homogeneous by TLC (9:1 MeOH/CH2Cl2), mass spectrum (FAB) m/e 773 (M+K)+.

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-432505845fda4bc2b35b9c1ceb2e42c0
出典メモuspto-grants-1995_05