反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
63 g. of 4-chloro-1-ethyl-3-methyl-1H-pyrazolo[3,4-b]-pyridine-5-carboxylic acid ethyl ester (0.235 mol.) are dissolved in 360 ml. of anhydrous tetrahydrofuran. Nitrogen is passed through the flask and while stirring and cooling with tap water, 5.2 g. of lithium aluminum hydride is added a bit at a time so that the reaction temperature does not exceed 25°. Stirring is continued for 2 hours at room temperature. Without further stirring, the reaction mixture is allowed to stand overnight. Then 300 ml. of 3N hydrochloric acid is added while stirring and cooling with ice water to keep the temperature between 15° and 20°. The clear solution is evaporated to dryness in vacuo, the residue is treated with 100 ml. of water and precipitated starting material (5-6 g.) is filtered off. Then the filtrate is diluted with 300 ml. of water and refrigerated overnight. The 4-chloro-1-ethyl-3-methyl-1H-pyrazolo[3,4-b]pyridine-5-methanol which crystallizes is filtered and dried at 70°, yield 32 g., m.p. 119°-121°. The compound is recrystallized from acetonitrile, m.p. 121°-122°. Acidification of the aqueous mother liquor with hydrochloric acid, evaporation in vacuo and extraction of the residue by means of boiling acetonitrile yields some starting material in form of the hydrochloride.
WORKUP
后处理
- customdoes not exceed 25°
- stirringStirring
- waitto stand overnight
- stirringwhile stirring
- customthe temperature between 15° and 20°
- customThe clear solution is evaporated to dryness in vacuo
- additionthe residue is treated with 100 ml
- customof water and precipitated
- filtrationis filtered off
- additionThen the filtrate is diluted with 300 ml
- customof water and refrigerated overnight
- customThe 4-chloro-1-ethyl-3-methyl-1H-pyrazolo[3,4-b]pyridine-5-methanol which crystallizes
- filtrationis filtered
- customdried at 70°
- customThe compound is recrystallized from acetonitrile, m.p. 121°-122°
- customAcidification of the aqueous mother liquor with hydrochloric acid, evaporation
- extractionin vacuo and extraction of the residue by means of boiling acetonitrile