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Chemical Structure| 89088-52-8 Chemical Structure| 89088-52-8

Structure of 89088-52-8

Chemical Structure| 89088-52-8

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Product Details of [ 89088-52-8 ]

CAS No. :89088-52-8
Formula : C10H12ClN3
M.W : 209.68
SMILES Code : CN1N=C(N2C(C)=CC=C2C)C=C1Cl

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* 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.

  • Upstream synthesis route of [ 89088-52-8 ]

[ 89088-52-8 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 89088-52-8 ]
  • [ 1191453-81-2 ]
YieldReaction ConditionsOperation in experiment
93% With hydroxylamine hydrochloride; potassium hydroxide In ethanol; water at 105℃; for 48 h; A Seal Tube was charged with 5-chloro-3-(2,5-dimethyl-1H-pyrrol-1-yl)-1- methyl-1H-pyrazole 76c (0.50 g, 2.38 mmol) in EtOH (20 mL) and hydroxylamine hydrochloride (0.83 g, 12.0 mmol) in EtOH (5 mL) drop wise followed by drop wise addition of potassium hydroxide (0.30 g, 6.0 mmol) dissolved in water (10 mL). The reaction mixture was heated at 105°C for 2 days. Reaction was monitored by TLC. Reaction mixture was concentrated fully to obtained crude, which was purified by column chromatography (Si02), eluting with 0-30percent EtOAc-hexane to obtain 5-chloro-1- methyl-1H-pyrazol-3-amine precursor-45 (0.29 g, 93percent yield) as yellow liquid. ‘H NMR (400 MHz, DMSO-d6): ö 5.49 (s, 1H), 4.74 (s, 2H), 3.51 (s, 3H).MS: 131.94 (M+H).
15% With hydroxylamine hydrochloride; potassium hydroxide In ethanol; water at 105℃; for 48 h; A mixture of hydroxylamine hydrochloride (608.5 mg, 8.75 mmol) in ethanol (6.5 mL) was treated with a solution of potassium hydroxide (247.6 mg, 4.41 mmol) in water (3.6 mL) and ethanol (3.6 mL) followed by addition of 5-chloro-3-(2,5-dimethyl-pyrrol-1-yl)-1-methyl-1H-pyrazole (0.36 g, 1.75 mmol). The resulting reaction mixture was heated in a sealed tube at 105° C. for 2 d. After this time, the reaction was cooled to 25° C. The reaction was then diluted with water (50 mL) and extracted with diethyl ether (3.x.50 mL) and methylene chloride (1.x.50 mL). The combined organics were washed with a saturated aqueous sodium bicarbonate solution (4.x.50 mL), water (1.x.50 mL), a saturated aqueous sodium chloride solution (1.x.50 mL), dried over magnesium sulfate, filtered, rinsed with methylene chloride and concentrated in vacuo. Silica gel column chromatography (AnaLogix, 40 g, 10-100percent ethyl acetate/hexanes) afforded 5-chloro-1-methyl-1H-pyrazol-3-ylamine (34.9 mg, 15percent) as an orange solid; ES+-HRMS m/e calcd for C4H6N4Cl [M+H+] 132.0323, found 132.0323.
References: [1] Patent: WO2015/25197, 2015, A1, . Location in patent: Paragraph 000153.
[2] Patent: US2009/264434, 2009, A1, . Location in patent: Page/Page column 43.
 

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