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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 514973생성일: 2026년 10월 24일

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/ko/reaction/514973

반응식

참여 물질

역할이름HCID투입량
반응물Pantothenic AcidHCID 6613—
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(2-(2-((2,6-Dichlorophenyl)amino)phenyl)acetyloxy)ethanamineHCID 76960476—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물[2-(2,6-Dichloro-phenylamino)-phenyl]-acetic acid 2-[3-((R)-2,4-dihydroxy-3,3-dimethyl-butyrylamino)-propionylamino]-ethyl esterHCID 9182768726.4%

반응 단계

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].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108942B1
출처 데이터셋uspto-grants-2015_08
ORD IDord-70afac8a5695494f86c31496194e923c
출처 메모uspto-grants-2015_08