HRID251687
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID8471
Triethylamine
C6H15N
HCID2723939
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
HCID12878164
Methyl 8-aminooctanoate--hydrogen chloride (1/1)
C9H20ClNO2
HCID136387977
4-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzoic acid
C16H10FN3O3
HCID178418300
未命名化合物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
4-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)benzoic acid (311 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), hydroxybenzo-triazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 8-aminocaprylic acid methyl ester hydrochloride (251 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 (290 mg, 62% yield) as a brown solid. LC-MS (m/z) 467 (M+1).
WORKUP
后处理
- additionwere added
- filtrationThe solids were collected by vacuum filtration
- washwashed with water
- customdried under vacuum