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Chemical Structure| 1181573-42-1 Chemical Structure| 1181573-42-1

Structure of 1181573-42-1

Chemical Structure| 1181573-42-1

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Product Details of [ 1181573-42-1 ]

CAS No. :1181573-42-1
Formula : C12H22N2O2
M.W : 226.32
SMILES Code : O=C(N1[C@](C2)([H])CC[C@]2([H])[C@H]1CN)OC(C)(C)C

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Application In Synthesis of [ 1181573-42-1 ]

* 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 [ 1181573-42-1 ]

[ 1181573-42-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1181573-42-1 ]
  • [ 166599-84-4 ]
  • [ 1181573-44-3 ]
YieldReaction ConditionsOperation in experiment
B.2 Synthesis of (lR^S^SJ-S-Acylaminomethyl-l-aza-bicycloβ.l.ljheptane derivatives; B.2.1 Synthesis of (lR^S^SJ-S-Acylaminomethyl^-aza-bicycloβJ.llheptane^- carboxylic acid tert-butyl ester derivatives; (general procedure); TBTU (0.73 mmol, 1.1 Oeq) is added to a solution of the respective carboxylic acid (0.70 mmol, 1.05eq) and DIPEA (1.66 mmol, 2.5eq) in DCM (1.0 mL) and DMF (0.25 mL). After 10 min a solution of (lR,3S,4S)-3-aminomethyl-2-aza-bicyclo[2.2.1]heptane-2- carboxylic acid tert-butyl ester (0.66 mmol, l.Oeq) in DCM (1.0 mL) is added and the mixture is stirred for 2h and washed twice with water (1.0 mL). The organic layer is dried over MgSO4, the solvents are removed in vacuo and the residue is purified by prep. HPLC to give the respective amide.; (lR,3S,4S)-3-[(Benzofuran-4-carbonyl)-amino]-methyl}-2-aza-bicyclo[2.2.1]heptane- 2-carboxylic acid tert-butyl ester prepared by reaction of (lR,3S,4S)-3-aminomethyl-2-aza-bicyclo[2.2.1]heptane-2- carboxylic acid tert-butyl ester with <strong>[166599-84-4]benzofuran-4-carboxylic acid</strong> (M.A. Eissenstat et al. J. Med. Chem. 1995, 38, 3094-3105). LC-MS (basic): tR = 0.97 min; [M+H]+ = 371.1.
 

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