돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251668생성일: 2026년 10월 26일

4-Chloro-1,2-diaminobenzene → 6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-N-(2-amino-4-chlorophenyl)hexanamide

https://huagongshe.com/reaction/251668

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-1,2-diaminobenzeneHCID 7263—
반응물TriethylamineHCID 8471—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-hexanoic acidHCID 136387951—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-N-(2-amino-4-chlorophenyl)hexanamideHCID 13638795571%

반응 단계

6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-hexanoic acid (441 mg, 1 mmol), and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (394 mg, 2 mmol), hydroxy-benzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 4-chloro-o-phenylenediamine (171 mg, 1.2 mmol) were added. The mixture was stirred for 24 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (402 mg, 71% yield) as a red solid. LC-MS (m/z) 566 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863315B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-afff7f5a5e5148418e4a15a667b50f37
출처 메모uspto-grants-2011_01