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HRID 514973作成日:2026年10月25日

Pantothenic Acid → [2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid 2-[3-((R)-2,4-dihydroxy-3,3-dimethyl-butyrylamino)-propionylamino]-ethyl ester

https://huagongshe.com/reaction/514973

反応式

関与物質

役割名称HCID仕込み量
反応物Pantothenic AcidHCID 6613—
反応物TriethylamineHCID 8471—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-(2-(2-((2,6-Dichlorophenyl)amino)phenyl)acetyloxy)ethanamineHCID 76960476—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物[2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid 2-[3-((R)-2,4-dihydroxy-3,3-dimethyl-butyrylamino)-propionylamino]-ethyl esterHCID 9182768726.4%

反応手順

To a stirred solution of 3-((R)-2,4-Dihydroxy-3,3-dimethyl-butyrylamino)-propionic acid 6 (0.2 g, 0.0007 mol, 1 eq) in DMF (4 mL) was added triethyl amine (0.31 g, 0.003 mol), EDC.HCl (0.22 g, 0.001 mol), HOBt (0.15 g, 0.001 mol) and [2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid 2-amino-ethyl ester 5 (0.26 g, 0.0007 mol, 1 eq) at rt. The resulting mixture was stirred at room temperature for 16 h. Reaction was monitored by TLC. After completion, reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (2×20 mL). Combined organic layer was dried over anhydrous Na2SO4 and evaporated under reduced pressure and purified by silica gel column chromatography using Methanol and DCM (3:97) to get 0.11 g (26.4% Yield) of CLX-SYN-G18-C01 as an off white solid; Mass: 539.9 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108942B1
出典データセットuspto-grants-2015_08
ORD IDord-70afac8a5695494f86c31496194e923c
出典メモuspto-grants-2015_08