HRID559787
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID311
Citric acid
C6H8O7
HCID81531
Diisopropylethylamine
C8H19N
HCID181649
3H-1,2,3-Triazolo[4,5-b]pyridine, 3-hydroxy-
C5H4N4O
HCID2729269
1-[4-(Methanesulfonyl)phenyl]methanamine--hydrogen chloride (1/1)
C8H12ClNO2S
HCID9886157
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
HCID11702104
6-METHYL-2-OXO-1-(3-(TRIFLUOROMETHYL)PHENYL)-1,2-DIHYDROPYRIDINE-3-CARBOXYLIC ACID
C14H10F3NO3
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A mixture of 6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxylic acid (7.43 g, 25 mmol), HATU (10.5 g, 27.5 mmol), HOAT (3.75 g, 27.5 mmol) and DIEA (14.2 ml, 82.5 mmol) in NMP (65 ml) was reacted for 1 h, then 4-methylsulphonylbenzyl amine hydrochloride (5.8 g, 26 mmol) was added. After 1 h, the reaction mixture was slowly poured into stirred ice water (1 L). A powder was formed, and the water mixture was acidified to pH 3 with citric acid (0.5 M), and stirring was continued for 1 h. The precipitate was filtered off, washed with water and dried in vacuum overnight. Recrystallisation from EtOAc gave 8.1 g (70%).
WORKUP
后处理
- customwas reacted for 1 h
- additionthe reaction mixture was slowly poured
- customA powder was formed
- waitwas continued for 1 h
- filtrationThe precipitate was filtered off
- washwashed with water
- customdried in vacuum overnight
- customRecrystallisation from EtOAc
- customgave 8.1 g (70%)