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Chemical Structure| 88654-17-5 Chemical Structure| 88654-17-5

Structure of 88654-17-5

Chemical Structure| 88654-17-5

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Product Details of [ 88654-17-5 ]

CAS No. :88654-17-5
Formula : C7H14N2S
M.W : 158.26
SMILES Code : S=C(C1CCN(C)CC1)N
MDL No. :MFCD11916054

Safety of [ 88654-17-5 ]

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

Application In Synthesis of [ 88654-17-5 ]

* 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 [ 88654-17-5 ]

[ 88654-17-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 214834-18-1 ]
  • [ 50-00-0 ]
  • [ 88654-17-5 ]
YieldReaction ConditionsOperation in experiment
To a suspension of ferf-butyl-4-carbamothioylpiperidine-1-carboxylate (prepared as described in Preparation 3, 2.65 g, 10.86 mmol) in dry dioxane (40 mL) a 4 M solution of HCI in dioxane was added (16 mL, 64 mmol, 5.9 eq) and the mixture was stirred at r.L After 1 h a further addition of HCI (10 mL) was made and stirring was continued for 2 more h. The solvent was evaporated to dryness and the residue was taken up with toluene and evaporated to dryness two times.The residue was dissolved in MeOH (64 mL) and aqueous formaldehyde (2 mL, 26.86 mmol, 2.5 eq) was added, followed by acetic acid (2.24 mL, 39.17 mmol, 3.6 eq) and sodium cyanoborohydride (2.08 g, 28.24 mmol, 2.6 eq) and the mixture was stirred at r.t. for 2 h. The solvent was then concentrated under reduced pressure and the residue was taken up with ethyl acetate, washed with aqueous saturated NaHC03 and brine, dried over Na2S04 and evaporated to dryness to give 2.2 g of the title compound as white solid.1H NMR (401 MHz, DMSO-d6) δ ppm 9.35 (br. s., 1 H), 9.08 (br. s., 1 H), 3.44 - 3.19 (m, 2 H), 2.86 (br. s., 2 H), 2.44 (t, J = 10.2 Hz, 1 H), 2.21 (br. s., 3 H), 1.82 - 1.73 (m, 2 H), 1.63 (d, J = 11.9 Hz, 2 H)HRMS (ESI) calcd for C7Hi5N2S [M+H]+ 159.0951 , found 159.0944.
2.2 g Preparation of 1-methylpiperidine-4-carbothioamide, cmpd. of formula 8 [R1=1-methyl-piperidin-4-yl] (Preparation 5, Methods A, D and E) To a suspension of tert-butyl-4-carbamothioylpiperidine-1-carboxylate (prepared as described in Preparation 3, 2.65 g, 10.86 mmol) in dry dioxane (40 mL) a 4 M solution of HCl in dioxane was added (16 mL, 64 mmol, 5.9 eq) and the mixture was stirred at r.t. After 1 h a further addition of HCl (10 mL) was made and stirring was continued for 2 more h. The solvent was evaporated to dryness and the residue was taken up with toluene and evaporated to dryness two times. The residue was dissolved in MeOH (64 mL) and aqueous formaldehyde (2 mL, 26.86 mmol, 2.5 eq) was added, followed by acetic acid (2.24 mL, 39.17 mmol, 3.6 eq) and sodium cyanoborohydride (2.08 g, 28.24 mmol, 2.6 eq) and the mixture was stirred at r.t. for 2 h. The solvent was then concentrated under reduced pressure and the residue was taken up with ethyl acetate, washed with aqueous saturated NaHCO3 and brine, dried over Na2SO4 and evaporated to dryness to give 2.2 g of the title compound as white solid. 1H NMR (401 MHz, DMSO-d6) δ ppm 9.35 (br. s., 1H), 9.08 (br. s., 1H), 3.44-3.19 (m, 2H), 2.86 (br. s., 2H), 2.44 (t, J=10.2 Hz, 1H), 2.21 (br. s., 3H), 1.82-1.73 (m, 2H), 1.63 (d, J=11.9 Hz, 2H) HRMS (ESI) calcd for C7H15N2S [M+H]+ 159.0951. found 159.0944.
 

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