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Chemical Structure| 179556-97-9 Chemical Structure| 179556-97-9

Structure of 179556-97-9

Chemical Structure| 179556-97-9

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Product Details of [ 179556-97-9 ]

CAS No. :179556-97-9
Formula : C14H28N2O2
M.W : 256.38
SMILES Code : O=C(N1CCC(NCC(C)C)CC1)OC(C)(C)C
MDL No. :MFCD12106420

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Application In Synthesis of [ 179556-97-9 ]

* 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 [ 179556-97-9 ]

[ 179556-97-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 179556-97-9 ]
  • [ 19415-51-1 ]
  • 4-[(5-fluoro-2-methoxy-benzyl)-isobutyl-amino]-piperidine-1-carboxylic acid <i>tert</i>-butyl ester [ No CAS ]
  • 2
  • [ 179556-97-9 ]
  • [ 90176-80-0 ]
  • [ 710971-52-1 ]
YieldReaction ConditionsOperation in experiment
With sodium tris(acetoxy)borohydride; In DMF (N,N-dimethyl-formamide); 1,2-dichloro-ethane; at 20℃; for 16h; To a solution of 4-isobutylamino-piperidine-1-carboxylic acid tert-butyl ester (10 g, 39mmol, 1.0 eq) in 1,2-dichloroethane (100 ml) was added 2- (trifluoromethyl)-4- fluorobenzaldehyde (22. 5G, 117mmol, 3.0 eq). To this was added a solution of sodium triacetoxyborohydride (24.8g, 117mmol, 3.0 eq) in dimethylformamide (20 ml). This mixture was left to stir under nitrogen, at room temperature, for 16 h. After this time the reaction mixture was quenched with water (50 ml) and subsequently stirred vigorously for several minutes. The reaction mixture was then separated with DCM, washing the organic layer with water (x3). The combined organics were dried over sodium sulfate and evaporated in vacuo to give an oil. Purification of this crude oil by chromatography on silica was then performed using an Isco system, eluting with 0-50% ethyl acetate: Hexane gradient conditions over 40 mins gave product which was taken directly onto the next step.
  • 3
  • [ 179556-97-9 ]
  • [ 10133-22-9 ]
  • [ 866328-90-7 ]
YieldReaction ConditionsOperation in experiment
100% With potassium carbonate; In acetonitrile; for 16h;Heating / reflux; To a solution of 5-bromomethyl-benzo [b] thiophene (1. 55g, 6.8mmol, 2.4 eq) and 1,1- dimethylethyl 4-[(2-methylpropyl) amino] piperidine-1-carboxylate (0. 71g, 2. 8mmol, 1 eq) in acetonitrile (25ml) is added potassium carbonate (0.62g, 4.4mmol, 1.6eq). The mixture is heated to reflux for 16 hours. The solution is filtered and the solvent removed in vacuo. The resulting oil is purified on a 40g Redisep column using a gradient of 0-20% ethyl acetate/iso-hexane to give 1, 1-dimethylethyl 4-f [ (1-benzothienyl-5-yl) methyl]- (2- methylpropyl) amino}-piperidine-l-carboxylate as an oil (1.12 g, 100 %). mass spectrum (LCMS): m/z= 403.5 (M++1), Rt= 3.38 (6 min gradient) ; 1H NMR (300 MHz, CDC13) : 8= 7. 80-7. 60 (2 H, m), 7.37-7. 33 (1 H, m), 7.32-7. 26 (1 H, m), 7.25-7. 20 (1 H, m), 4.17- 3.94 (2 H, m), 3.65 (2 H, s), 2. 65-2. 36 (3 H, m), 2.24-2. 10 (2 H, d), 1.71-1. 28 (5 H, m), 1.38 (9 H, s), 0.88-0. 69 (6 H, d).
46% With potassium carbonate; In acetonitrile; Add potassium carbonate (0.619 g, 4.4 mmol, 1.6 eq) followed by 5-bromomethyl- benzo [b] thiophene (17.7 g, 78 mmol, 1 eq) in one portion to a stirred solution of 1,1- dimethylethyl 4- [ (2-methylpropyl) amino] piperidine-1-carboxylate (20 g, 78 mmol, 1 eq) in acetonitrile (400 ml). Cool, add water (250 ml) then filter. Wash the solid with ice cold acetonitrile and leave to dry on sinter for 1 hr. Purify on a 330 g Redisep column (20 g per column) using a gradient of 0-40% Ethyl acetate/iso-hexane to give 1,1- dimethylethyl 4- { [ (l-benzothienyl-5-yl] methyl]- (2-methylpropyl) amino}-piperidine-1- carboxylate (7.64 g, 46 %) as yellow solid. LCMS Rt= 3.38 (6 min gradient) M++1 : 403.5. 1H NMR (300 MHz, CDC13) 6 ppm 7.80-7. 60 (2 H, m), 7.37-7. 33 (1 H, m), 7.32- 7.26 (1 H, m), 7.25-7. 20 (1 H, m), 4.17-3. 94 (2 H, m), 3.65 (2 H, s), 2.65-2. 36 (3 H, m), 2.24-2. 10 (2 H, d), 1.71-1. 28 (5 H, m), 1.38 (9 H, s), 0.88-0. 69 (6 H, d).
 

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