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Chemical Structure| 236406-15-8 Chemical Structure| 236406-15-8

Structure of 236406-15-8

Chemical Structure| 236406-15-8

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Product Details of [ 236406-15-8 ]

CAS No. :236406-15-8
Formula : C14H20N2O2
M.W : 248.32
SMILES Code : O=C(OCC1=CC=CC=C1)NC2(C)CCNCC2
MDL No. :MFCD03265498

Safety of [ 236406-15-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 236406-15-8 ]

* 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 [ 236406-15-8 ]

[ 236406-15-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 236406-15-8 ]
  • [ 676560-01-3 ]
  • 4-benzyloxycarbonylamino-4-methyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid tert-butyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
In 1,4-dioxane; hexane; Example 40B 4-Amino-4-methyl-3, 4, 5, 6-tetrahydro-2H-(1,2') bipyridinyl-5'-carboxylic acid tert-butyl ester To a stirred solution of (4-methyl-piperidin-4-yl)-carbamic acid benzyl ester (0.31 g, 1.28 mmol, Example 30B) in dioxane (5.0 mL) at room temperature was added <strong>[676560-01-3]6-fluoro-nicotinic acid tert-butyl ester</strong> (0.21 g, 1.07 mmol). The reaction mixture was stirred at 80 C. for 18 hours, concentrated under reduced pressure and purified by flash chromatography with 10% to 30% ethyl acetate in hexane to provide 4-benzyloxycarbonylamino-4-methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-5'-carboxylic acid tert-butyl ester. MS (CI) m/z 426 (M+1)+; 1H NMR (300 MHz, CDCl3) delta ppm 8.74(d, 1H), 7.97 (dd, 1H), 7.35 (m, 5H), 7.26 (s, 1H), 5.07 (s, 2H), 4.68 (s, 1H), 3.97 (m, 2H), 3.37 (m, 2H), 2.08 (m, 2H), 1.66 (m, 2H), 1.56 (s, 9H), 1.42 (s, 3H).
In 1,4-dioxane; hexane; Example 40B 4-Amino-4-methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-5'-carboxylic acid tert-butyl ester To a stirred solution of (4-methyl-piperidin-4-yl)-carbamic acid benzyl ester (0.31 g, 1.28 mmol, Example 30B) in dioxane (5.0 mL) at room temperature was added <strong>[676560-01-3]6-fluoro-nicotinic acid tert-butyl ester</strong> (0.21 g, 1.07 mmol). The reaction mixture was stirred at 80 C. for 18 hours, concentrated under reduced pressure and purified by flash chromatography with 10% to 30% ethyl acetate in hexane to provide 4-benzyloxycarbonylamino-4methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-5'-carboxylic acid tert-butyl ester. MS (CI) m/z 426 (M+1)+; 1H NMR (300 MHz, CDCl3) delta ppm 8.74(d, 1H), 7.97 (dd, 1H), 7.35 (m, 5H), 7.26 (s, 1H), 5.07 (s, 2H), 4.68 (s, 1H), 3.97 (m, 2H), 3.37 (m, 2H), 2.08 (m, 2H), 1.66 (m, 2H), 1.56 (s, 9H), 1.42 (s, 3H).
In 1,4-dioxane; at 20 - 80℃; for 18.0h; To a stirred solution of (4-methyl-piperidin-4-yl) -carbamic acid benzyl ester (0.31 g, 1.28 mmol, Example 30B) in dioxane (5.0 mL) at room temperature was added 6-fluoro- nicotinic acid tert-butyl ester (0.21 g, 1.07 [MMOL).] The reaction mixture was stirred at 80 [C] for 18 hours, concentrated under reduced pressure and purified by flash chromatography with 10% to 30% ethyl acetate in hexane to provide 4-benzyloxycarbonylamino-4-methyl-3,4, 5,6- [TETRAHYDRO-2H- (1, 2') BIPYRIDINYL-5'-CARBOXYLIC] acid tert-butyl ester. MS (CI) m/z 426 (M+1) [+] ; [JH] NMR (300 MHz, CDC13) 8 ppm 8.74 (d, [1H),] 7.97 (dd, 1H), 7.35 [(M,] [5H),] 7.26 (s, [1H),] 5.07 (s, 2H), 4.68 (s, [1H),] 3.97 (m, 2H), 3.37 [(M,] 2H), 2.08 [(M,] 2H), 1.66 (m, 2H), 1.56 (s, 9H), 1.42 (s, 3H). To a stirred solution [OF 4-BENZYLOXYCARBONYLAMINO-4-METHYL-3, 4, 5, 6-TETRAHYDRO-2H-] (1, 2') [BIPYRIDINYL-5'-CARBOXYLIC] acid tert-butyl ester (0.29 g, 0.68 mmol) in isopropanol, methanol and ethyl acetate (1: 1: 1,5. 0 mL) at room temperature was added ammonium formate (0.25 g, 1.07 mmol) and 10% Pd/C (25 mg) under nitrogen. The reaction mixture was stirred at 80 [C] for 30 minutes, cooled, filtered through Celite, and concentrated under reduced pressure to provide the titled compound. MS (CI) m/z 292 (M+1) [+] [;'H] NMR (300 MHz, methanol-d4) [8] ppm 8.61 (d, [1H),] 7.95 (d, d [1H),] 6.79 (d, [1H),] 4.80 (s, 2H), 3.85-3. 79 [(M,] 2H), 3.66-3. 60 [(M,] 2H), 1.67-1. 59 (m, 4H), 1.58 (s, 9H), 1.23 (s, 3H).
 

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