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Chemical Structure| 886362-07-8 Chemical Structure| 886362-07-8

Structure of 886362-07-8

Chemical Structure| 886362-07-8

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Product Details of [ 886362-07-8 ]

CAS No. :886362-07-8
Formula : C8H9N3O
M.W : 163.18
SMILES Code : NC1=NNC2=C1C(OC)=CC=C2
MDL No. :MFCD08276946
InChI Key :JZAMRGWQDJMEJD-UHFFFAOYSA-N
Pubchem ID :18526053

Safety of [ 886362-07-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 886362-07-8 ]

* 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.

  • Downstream synthetic route of [ 886362-07-8 ]

[ 886362-07-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 94088-46-7 ]
  • [ 886362-07-8 ]
YieldReaction ConditionsOperation in experiment
92% With hydrazine hydrate; In butan-1-ol; for 18h;Reflux; Inert atmosphere; Intermediate 14-(Methyloxy)-1H-indazol-3-amine; A mixture of <strong>[94088-46-7]2-fluoro-6-(methyloxy)benzonitrile</strong> (available from Apollo) (10 g, 66 mmol) and hydrazine hydrate (9.63 mL, 198 mmol) in n-butanol (100 mL) was heated at reflux under nitrogen for 18 hours. The reaction mixture was allowed to cool, water (300 mL) was added, and the organic phase was removed. The solid in the aqueous phase was collected by filtration and dried in vacuo at 40 C. to give a white solid (0.6 g). The butanol phase was evaporated in vacuo, and the residue and the aqueous mother liquors were combined and extracted using ethyl acetate (2×200 mL). The combined ethyl acetate extractions were dried over magnesium sulphate and evaporated in vacuo. The residue was dissolved in DCM and applied to a 100 g silica cartridge. This was eluted with cyclohexane (500 ml), cyclohexane-ethyl acetate (1:1 v/v, 500 mL) and ethyl acetate (500 mL). The required fractions were combined and evaporated in vacuo to give the title compound (9.92 g, 92%) as an off-white solid. LCMS (System A) RT=0.5 min, ES+ve m/z 164 (M+H)+.
92% With hydrazine hydrate; In butan-1-ol; for 18h;Reflux; Inert atmosphere; Intermediate 94-(Methyloxy)-1 H-indazol-3-amineA mixture of <strong>[94088-46-7]2-fluoro-6-(methyloxy)benzonitrile</strong> (available from Apollo) (10 g, 66 mmol) and hydrazine hydrate (9.63 mL, 198 mmol) in n-butanol (100 mL) was heated at reflux under nitrogen for 18 hours. The reaction mixture was allowed to cool, water (300 mL) was added, and the organic phase was removed. The solid in the aqueous phase was collected by filtration and dried in vacuo at 40C to give a white solid (0.6g). The butanol phase was evaporated in vacuo, and the residue and the aqueous mother liquors were combined and extracted using ethyl acetate (2 x 200 mL). The combined ethyl acetate extractions were dried over magnesium sulphate and evaporated in vacuo. The residue was dissolved in DCM and applied to a 100g silica cartridge. This was eluted with cyclohexane (500 ml), cyclohexane-ethyl acetate (1 : 1v/v, 500 mL) and ethyl acetate (500 mL). The required fractions were combined and evaporated in vacuo to give the title compound (9.92 g, 92%) as an off-white solid. LCMS (System A) RT = 0.5 min, ES+ve m/z 164 (M+H)+.
92% With hydrazine hydrate; In butan-1-ol; for 18h;Reflux; Inert atmosphere; A mixture of <strong>[94088-46-7]2-fluoro-6-(methyloxy)benzonitrile</strong> (available from Apollo) (10 g, 66 mmol) and hydrazine hydrate (9.63 mL, 198 mmol) in n-butanol (100 mL) was heated at reflux under nitrogen for 18 hours. The reaction mixture was allowed to cool, water (300 mL) was added, and the organic phase was removed. The solid in the aqueous phase was collected by filtration and dried in vacuo at 40C to give a white solid (0.6g). The butanol phase was evaporated in vacuo, and the residue and the aqueous mother liquors were combined and extracted using ethyl acetate (2 x 200 mL). The combined ethyl acetate extractions were dried over magnesium sulphate and evaporated in vacuo. The residue was dissolved in DCM and applied to a 100g silica cartridge. This was eluted with cyclohexane (500 ml), cyclohexane-ethyl acetate (1 : 1v/v, 500 mL) and ethyl acetate (500 mL). The required fractions were combined and evaporated in vacuo to give the title compound (9.92 g, 92%) as an off-white solid. LCMS (System A) RT = 0.5 min, ES+ve m/z 164 (M+H)+.
44% With hydrazine hydrate; In butan-1-ol; for 7h;Reflux; General procedure: The title compounds were obtained according to the procedure described by Vasudevan et al.18 A solution of the commercially available 2-fluorobenzonitrile (1d-e, j-k) (22.0 mmol) and 98% hydrazine hydrate (90.0 mmol) in n-butanol (15 ml) was stirred under reflux for 7 h. After cooling to room temperature, the resulting mixture was concentrated under reduced pressure to a volume of 5 ml, and then water was added. The solid product that was precipitated was filtered, washed with water, dried and purified by crystallization from methanol. In this manner, the following compounds were obtained.

 

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