113209-90-8 | Pyridine-derivatives

Extracurricular laboratory: Synthetic route of (4-Chloro-5-fluoropyridin-2-yl)methanol

At the same time, in my other blogs, there are other synthetic methods of this type of compound,113209-90-8, (4-Chloro-5-fluoropyridin-2-yl)methanol, and friends who are interested can also refer to it.

Application of 113209-90-8, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 113209-90-8, name is (4-Chloro-5-fluoropyridin-2-yl)methanol. A new synthetic method of this compound is introduced below.

(v) Substituting 2-hydroxymethyl-4-chloro-5-fluoropyridine (2.5 g) for 2-hydroxymethyl-3-fluoro-4-chloropyridine and using corresponding molar proportions of the other reagents in the method of Example 27(v), gave 2-hydroxymethyl-4-morpholino-5-fluoropyridine (2.08 g) m.p. 134-136 (from acetonitrile).

Reference:
Patent; SmithKline & French Laboratories Limited; US5250527; (1993); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

New downstream synthetic route of 113209-90-8

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 113209-90-8, (4-Chloro-5-fluoropyridin-2-yl)methanol.

Synthetic Route of 113209-90-8, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 113209-90-8, name is (4-Chloro-5-fluoropyridin-2-yl)methanol, molecular formula is C6H5ClFNO, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

(i) Substituting 2-hydroxymethyl-4-chloro-5-fluoropyridine (2.5 g) for 2-hydroxymethyl-3-fluoro-4-chloropyridine and using corresponding molar proportions of the other reagents in the method of Example 31(i) gave 2-hydroxymethyl-4-dimethylamino-5-fluoropyridine (2.18 g) m.p. 80-82.

Reference:
Patent; SmithKline & French Laboratories Limited; US5250527; (1993); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

New downstream synthetic route of 113209-90-8

Reference:
Patent; SmithKline & French Laboratories Limited; US5250527; (1993); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Analyzing the synthesis route of (4-Chloro-5-fluoropyridin-2-yl)methanol

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,113209-90-8, its application will become more common.

Synthetic Route of 113209-90-8 ,Some common heterocyclic compound, 113209-90-8, molecular formula is C6H5ClFNO, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

A mixture of 6′-[3-(dimethylamino)-1-pyrrolidinyl]-4-hydroxy-2/-/-1 ,3′-bipyridin-2-one (150 mg, 0.499 mmol) and triphenylphosphine (327 mg, 1.249 mmol) was treated with (4-chloro-5-fluoro-2-pyridinyl)methanol (81 mg, 0.499 mmol) dissolved in dichloromethane (5 ml). Bis(1 ,1-dimethylethyl) (E)-1 ,2-diazenedicarboxylate (287 mg, 1.249 mmol) was added in two portions, and the reaction mixture was stirred at 250C for 2 h then concentrated under a stream of nitrogen gas. Purification by reverse phase HPLC (1 to 50% gradient) and concentration of the fractions containing product provided a residue. The residue was treated with aqueous NaHCO3 solution and extracted with ethyl acetate. The organic layer was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo to provide the title compound as a white solid (1 14 mg, 51 %): 1H NMR (400 MHz, CDCI3) delta ppm 8.46 (s, 1 H), 8.06 (d, J = 2.7 Hz, 1 H), 7.56-7.48 (m, 2 H), 7.21 (d, J = 7.6 Hz, 1 H), 6.43 (d, J = 9.0 Hz, 1 H), 6.09 (dd, J = 7.4, 2.5 Hz, 1 H), 5.98 (d, J = 2.7 Hz, 1 H), 5.10 (s, 2 H), 3.95-3.84 (m, 1 H), 3.77-3.65 (br m, 2H), 3.55-3.22 (br m, 2 H), 2.60 (br s, 6 H), 2.47-2.29 (br m, 2 H); ES-LCMS m/z 444 {M+H)+.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,113209-90-8, its application will become more common.

Reference:
Patent; GLAXO GROUP LIMITED; WO2009/76387; (2009); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

A new synthetic route of 113209-90-8

With the rapid development of chemical substances, we look forward to future research findings about 113209-90-8.

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 113209-90-8, name is (4-Chloro-5-fluoropyridin-2-yl)methanol, molecular formula is C6H5ClFNO, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. Application In Synthesis of (4-Chloro-5-fluoropyridin-2-yl)methanol

To a solution of Intermediate 47 (200 mg) in CH2Cl2 (5 ml) was added manganese oxide (861 mg). The suspension was stirred overnight and filtered eluting with CH2Cl2. The filtrate was concentrated in vacuo to afford 130 mg (66%) of the title compound as a yellow oil. 1H-NMR (delta, ppm, CDCl3): 10.00 (s, 1 H), 8.64 (s, 1 H), 8.06 (d, 1 H).

With the rapid development of chemical substances, we look forward to future research findings about 113209-90-8.

Reference:
Patent; GLAXO GROUP LIMITED; EP2080761; (2009); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem