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Chemical Structure| 863679-83-8 Chemical Structure| 863679-83-8

Structure of 863679-83-8

Chemical Structure| 863679-83-8

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Product Details of [ 863679-83-8 ]

CAS No. :863679-83-8
Formula : C16H20BrNO2
M.W : 338.24
SMILES Code : O=C(N1CC2CC2(C1)C3=CC=C(C=C3)Br)OC(C)(C)C
MDL No. :MFCD10700129

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Application In Synthesis of [ 863679-83-8 ]

* 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 [ 863679-83-8 ]

[ 863679-83-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 863679-83-8 ]
  • [ 486460-21-3 ]
  • [ 1259556-59-6 ]
YieldReaction ConditionsOperation in experiment
62% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; for 6h;Reflux; To a solution of l-(4-bromo-phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (Intermediate I, 400 mg, 1.18 mmol) in anhydrous toluene (5 mL) were added Pd2(dba)3 (5.4 mg, 0.006 mmol), BINAP (11.0 mg, 0.018 mmol), sodium tert-butoxide (227 mg, 2.34 mmol) and 3-trifluoromethyl-5,6,7,8-tetrahydro-[l,2,4]triazolo[4,3-a]pyrazine (prepared by the procedure as described in reference J. Med. Chem., 2005, 48, 141-151) (340 mg, 1.77 mmol) at r.t. and reaction mixture was refluxed for 6h. Reaction mixture was then concentrated and the crude product was purified by column chromatography (silica gel, 6: 4 EtOAc: Pet. ether) to afford the title compound as white solid (330 mg, 62%). ESIMS (m/z): 472.9 (M+23), 451.9 (M+2), 450.8 (M+l).
62% With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); In toluene; at 20℃; for 6h;Reflux; Step 1: Preparation of 1-[4-(3-trifluoromethyl-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl)-phenyl]-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl esterTo a solution of 1-(4-bromo-phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (Intermediate I, 400 mg, 1.18 mmol) in anhydrous toluene (5 mL) were added Pd2(dba)3 (5.4 mg, 0.006 mmol), BINAP (11.0 mg, 0.018 mmol), sodium tert-butoxide (227 mg, 2.34 mmol) and <strong>[486460-21-3]3-trifluoromethyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine</strong> (prepared by the procedure as described in reference J. Med. Chem., 2005, 48, 141-151) (340 mg, 1.77 mmol) at r.t. and reaction mixture was refluxed for 6 h. Reaction mixture was then concentrated and the crude product was purified by column chromatography (silica gel, 6:4 EtOAc:Pet. ether) to afford the title compound as white solid (330 mg, 62%).ESIMS (m/z): 472.9 (M+23), 451.9 (M+2), 450.8 (M+1).
 

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