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HomeProductsPharmaceutical IntermediatesAnti-Rheumatoid ArthritisSynthesis JAK1 and JAK2 Inhibitor Baricitinib Intermediate CAS 1029716-44-6
Synthesis JAK1 and JAK2 Inhibitor Baricitinib Intermediate CAS 1029716-44-6
  • Synthesis JAK1 and JAK2 Inhibitor Baricitinib Intermediate CAS 1029716-44-6

Synthesis JAK1 and JAK2 Inhibitor Baricitinib Intermediate CAS 1029716-44-6

    Payment Type: L/C,T/T
    Incoterm: FOB,CIF
    Min. Order: 1 Kilogram
    Delivery Time: 25 Days

Basic Info

Model No.: 1029716-44-6

Grade Standard: Medicine Grade

State: Solid

Additional Info

Packaging: 25KGS/DRUM

Productivity: Custom Manufacturing

Brand: VOLSENCHEM

Transportation: Air

Place of Origin: CHINA

Supply Ability: In stock

Product Description

Baritinib intermediate is 1-(1-ethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole CAS number 1029716-44-6. There are two main synthetic methods, the first one is use 4-bromo-1-(1-ethoxyethyl)-1H-pyrazole and 2-methoxy-4,4,5,5-four Methyl-1,3,2-dioxaborolan as the starting material, and the target product is obtained by one-step reaction. The yield of this method is only 50%. The second type: 4-bromo-1-(1-ethoxyethyl)-1H-pyrazole and boranoic acid pinacol ester are used as raw materials to obtain the target product through one-step reaction. The yield of this method is only 65. %. The yields of the above two methods are not ideal.

One method is ideal, in the presence catalyst of 0.1 equivalent of Boron trifluoride etherate, 1 equivalent of 2-chloromalonaldehyde is added to the toluene solvent and heated to 80-120, and the reaction is carried out to obtain 4-chloropyrazole, spin dry After the solvent, anhydrous ethanol, 2.0 equivalents of tetrahydroxydiboron, 3.0 equivalents of diisopropylethylamine, 0.05 equivalents of NiCl2 and 0.10 equivalents of PPh3 are directly added, followed by reaction at 20-80for 4-16 hours, and the inorganic particles are filtered off by cooling. The salt and the filtrate are evaporated to dryness. After adding ethyl acetate, the mixture is washed with water, and the organic layer is added with 1.2-1.5 equivalents of pinacol. After the reaction is completed, the mixture is washed with water, and the organic layer is filtered through celite, and mixed with a solvent to obtain the desired product. 1-(1-ethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole CAS number 1029716-44-6.

Thera Category: JAK Inhibitor

Cas No.: 1029716-44-6

Synonym1-(1-Ethoxyethyl)-1H-pyrazole-4-boronic acid pinacol ester;1-(1-ethoxyethyl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyrazole;:1-(1-ethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole;1H-Pyrazole, 1-(1-ethoxyethyl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;1-(1-ethoxyethyl)-4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole;(1-(1-ethoxyethyl)-1H-pyrazol-4-yl)boronic acid;

1029716-44-6

Molecular Formula: C13H23BN2O3

Molecular Weight: 266.14432

Specifications: Available on request

Packing:Export worthy packing

Material Safety Data Sheet:Available on request

Related intermediates:

1) Pyrazole-4-Boronic Acid Pinacol Ester CAS 269410-08-4

2) 1-Boc-3-(Cyanomethylene)Azetidine CAS 1153949-11-1

3) 4-Chloro-5H-pyrrolo[3,2-d]pyrimidine CAS 84905-80-6

4) 4-Chloro-7-((2-(Trimethylsilyl)ethoxy)Methyl)-7H-Pyrrolo[2,3-d]pyrimidine CAS 941685-26-3

5) (4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl Pivalate CAS 1146629-75-5

6) [4-(1H-Pyrazol-4-yl)-7H-Pyrrolo[2,3-d]pyrimidin-7-yl]methyl Pivalate CAS 1146629-77-7

7) Baricitinib (LY3009104, INCB028050) CAS 1187594-09-7

8) 2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile CAS 1187595-85-2

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