Structure of 109371-20-2
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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CAS No. : | 109371-20-2 |
Formula : | C8H10ClNO |
M.W : | 171.62 |
SMILES Code : | [O-][N+]1=CC(C)=C(Cl)C(C)=C1C |
MDL No. : | MFCD00277471 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
100% | At 90-95 0C, a solution of 4-chloro-2,3,5-trimethylpyridine-Lambda/-oxide (60.0 g, 350 mmol) in toluene (920 mL), which was kept at about 60 0C, was added over 7 h to acetic anhydride (232 mL). Under vacuum at about 60 0C, the reaction mixture was concentrated until 820 mL had been distilled off. Toluene (840 mL) was added and, again, solvents were distilled off (940 mL). Then, toluene (180 mL) and 40percent aqueous NaOH (80 mL) were added before the reaction mixture was heated at 50 0C for about 15 h. After addition of saturated aqueous sodium bicarbonate (120 mL), the phases were separated and the aqueous layer was extracted once more with toluene (80 mL). Finally, the combined organic phase was washed with saturated aqueous sodium bicarbonate (120 mL) and evaporated to dryness to give 4-chloro-2-hydroxymethyl-3,5-dimethylpyridine as a brownish oil which solidified upon standing; yield 61.8 g (quantitative).1H-NMR (200 MHz, DMSO-d6): delta= 2.30 (s, 3H), 2.36 (s, 3H), 4.58 (br s, 2H), 5.11 (br s, 1H), 8.27 (s, 1 H); LC-MS: MH+ = 172/174. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With potassium hydroxide; In toluene; for 6.25h; | (4) 4-(2,2-dimethyl-1,3-dioxan-5-ylmethoxy)-2,3,5-trimethylpyridine1-oxide A mixture of 4-chloro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1,3-dioxan-5-yl)methanol (688 g) and toluene (2.52 L) was heated under reflux while removing a water content. While azeotropical dehydration was continued, potassium hydroxide (0.58 kg) was added to the reaction mixture over 3 hours and 45 minutes, and azeotropic dehydration was continued for 2.5 hours. The mixture was cooled to 30° C. or less, and ethyl acetate (2.5 L) and a 17percent saline solution (3.5 L) were added to the mixture and then the mixture was allowed to stand for overnight. The ethyl acetate layer was separated and the aqueous layer was extracted with ethyl acetate (1.0 L*3). The ethyl acetate layers were combined, filtrated through celite, and concentrated under reduced pressure to obtain a desired product (1.20 kg). | |
A mixture of 4-chloro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1,3-dioxan-5-yl)methanol (688 g) and toluene (2.52 L) was heated to reflux while removing moisture. While continuing the azeotropic dewatering, the mixture was charged with potassium hydroxide (0.58 kg) over 3 hours and 45 minutes, and the azeotropic dewatering was then continued for another 2.5 hours. The reaction system was cooled to 30°C or less and then charged with ethyl acetate (2.5 L) and 17percent saline solution (3.5 L). The resultant solution was left to stand overnight. The ethyl acetate layer was collected, and the aqueous layer was extracted with ethyl acetate (1.0 L .x. 3). The combined ethyl acetate layers were filtered with Celite and then concentrated under reduced pressure to obtain 1.20 kg of the title compound. | ||
With potassium hydroxide; In toluene; for 6.25h;azeotropic dehydration; | A mixture of 4-nitro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1,3-dioxane-5-yl) methanol (688 g) and toluene (2.52 L) was refluxed while removing water. Potassium hydroxide (0.58 kg) was added thereto over 3 hours 45 minutes while continuing azeotropic dehydration followed by further continuing azeotropic dehydration for 2.5 hours. The reaction mixture was cooled to 30°C or lower followed by the addition of ethyl acetate (2.5 L) and 17percent brine (3.5 L) and allowing to stand undisturbed overnight. The ethyl acetate layer was isolated and the aqueous layer was extracted with ethyl acetate (1.0 L x 3). The combined ethyl acetate layer was filtered through Celite followed by concentrating under a reduced pressure to obtain 1.20 kg of the target substance. |
(Production Example 5) 4-(2,2-dimethyl-1,3-dioxan-5-yl)methoxy-2,3,5-trimethylpyridine 1-oxide [Show Image] A mixture of 4-chloro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1,3-dioxan-5-yl)methanol (688 g) and toluene (2.52 L) was heated to reflux with removing the water. Potassium hydroxide (0.58 kg) was added over a period of 3 hours and 45 minutes while carrying out azeotropic dehydration, and azeotropic dehydration was continued for 2.5 hours. The reaction system was cooled to blow 30°C, and then ethyl acetate (2.5 L) and a 17percent aqueous solution of sodium chloride (3.5 L) were added and the mixture was allowed to stand overnight. The ethyl acetate layer was separated off and the aqueous layer was extracted with ethyl acetate (1.0 L x 3). The combined ethyl acetate layers were filtered through celite and then concentrated under reduced pressure to produce 1.20 kg of the target substance. | ||
With potassium hydroxide; In toluene; for 6.25h;Heating / reflux; | (5) 4-(2.2-Dimethyl-1 ,3-dioxan-5-ylmethoxy)-2.3,5-trimethylpyridine 1 -oxideA mixture of 4-chloro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1 ,3-dioxan-5-yl)methanol (688 g), and toluene (2.52 L) was heated and refluxed while removing water. While continuing the azeotropic dehydration, potassium hydroxide (0.58 kg) was added thereto over 3 hours 45 minutes, and then the azeotropic dehydration was continued for a further 2.5 hours. The reaction system was then cooled to below 30 0C, ethyl acetate (2.5 L) and 17percent brine solution <n="43"/>(3.5 L) were added thereto, and the reaction system was allowed to stand overnight. The ethyl acetate layer was separated off, and the aqueous layer was subjected to extraction with ethyl acetate (1.0 L x 3). The ethyl acetate layers were combined, and filtered through Celite, and then vacuum concentration was carried out, whereby 1.20 kg of the target substance was obtained. |
Tags: 109371-20-2 synthesis path| 109371-20-2 SDS| 109371-20-2 COA| 109371-20-2 purity| 109371-20-2 application| 109371-20-2 NMR| 109371-20-2 COA| 109371-20-2 structure
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