反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrochloric Acid
ClH
Water
H2O
Triethylamine
C6H15N
Sodium Hydroxide
HNaO
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
4-(Methoxycarbonyl)bicyclo[2.2.2]octane-1-carboxylic acid
C11H16O4
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
5,6-Diamino-1-propyl-1H-pyrimidine-2,4-dione hydrochloride salt (570 mg) was dissolved in 20 mL of DMF along with bicyclo[2.2.2]octane-1,4-dicarboxylic acid monomethyl ester (520 mg, 2.45 mmol). HATU (980 mg, 1.05 eq) was added, followed by Et3N (1.40 mL, 4.05 eq). The resulting reaction mixture was stirred at rt overnight. The following morning, the reaction mixture was filtered to remove some of the precipitate. The filtrate was concentrated under reduced pressure. The resulting residue was dissolved in 10 mL of H2O containing 10 eq of NaOH (980 mg). The reaction mixture was stirred under reflux for 2 h. It was then cooled to rt and acidified to pH2 with concentrated HCl. The resulting precipitate was collected by filtration and dried to afford 680 mg of the acid derivative.
WORKUP
后处理
- customThe resulting reaction mixture
- filtrationThe following morning, the reaction mixture was filtered
- customto remove some of the precipitate
- concentrationThe filtrate was concentrated under reduced pressure
- stirringThe reaction mixture was stirred
- temperatureunder reflux for 2 h
- temperatureIt was then cooled to rt
- filtrationThe resulting precipitate was collected by filtration
- customdried