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Chemical Structure| 1595275-71-0 Chemical Structure| 1595275-71-0
Chemical Structure| 1595275-71-0

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Product Details of SG3199

CAS No. :1595275-71-0
Formula : C33H36N4O6
M.W : 584.66
SMILES Code : O=C1C2=CC(OC)=C(OCCCCCOC3=C(OC)C=C4C(N=C[C@@](CC(C)=C5)([H])N5C4=O)=C3)C=C2N=C[C@@]6([H])N1C=C(C)C6
English Name :(11aS,11a'S)-8,8'-(Pentane-1,5-diylbis(oxy))bis(7-methoxy-2-methyl-1,11a-dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepin-5-one)
MDL No. :MFCD34469130

Safety of SG3199

Application In Synthesis of SG3199

* 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 [ 1595275-71-0 ]

[ 1595275-71-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1595275-71-0 ]
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Stage #1: SG3199; 2,5-dioxopyrrolidin-1-yl cis-(E)-6-((((2,5-dioxopyrrolidin-1-yl)oxy)carbonyl)oxy)-1-methylcyclooct-4-ene-1-carboxylate With benzotriazol-1-ol In N,N-dimethyl-formamide at 20℃; Stage #2: With water; lithium hydroxide In methanol; N,N-dimethyl-formamide at 20℃; 5 [0345] TCO-PBD (12). To a solution of SG3199 in DMF is added bis-NHS-TCO 11 and HOBt. The reaction mixture is stirred at ambient temperature protected from light until the starting material is consumed. To the reaction mixture is added lithium hydroxide (solution in water) and methanol and the resulting solution is stirred for additional time at ambient temperature. The reaction mixture is then concentrated under reduced pressure and the resulting residue is purified by reverse phase chromatography (10-100% MeCN/water with 0.1% ammonium formate) to yield the desired product Compound 5.
Stage #1: SG3199; 2,5-dioxopyrrolidin-1-yl cis-(E)-6-((((2,5-dioxopyrrolidin-1-yl)oxy)carbonyl)oxy)-1-methylcyclooct-4-ene-1-carboxylate With benzotriazol-1-ol In N,N-dimethyl-formamide at 20℃; Stage #2: With water; lithium hydroxide In methanol; N,N-dimethyl-formamide at 20℃; 5 [0345] TCO-PBD (12). To a solution of SG3199 in DMF is added bis-NHS-TCO 11 and HOBt. The reaction mixture is stirred at ambient temperature protected from light until the starting material is consumed. To the reaction mixture is added lithium hydroxide (solution in water) and methanol and the resulting solution is stirred for additional time at ambient temperature. The reaction mixture is then concentrated under reduced pressure and the resulting residue is purified by reverse phase chromatography (10-100% MeCN/water with 0.1% ammonium formate) to yield the desired product Compound 5.
Stage #1: SG3199; 2,5-dioxopyrrolidin-1-yl cis-(E)-6-((((2,5-dioxopyrrolidin-1-yl)oxy)carbonyl)oxy)-1-methylcyclooct-4-ene-1-carboxylate With benzotriazol-1-ol In N,N-dimethyl-formamide at 20℃; Stage #2: With water; lithium hydroxide In methanol; N,N-dimethyl-formamide at 20℃; 5 CO-PBD (12). To a solution of SG3199 in DMF is added bis-NHS-TCO 11 and HOBt. The reaction mixture is stirred at ambient temperature protected from light until the starting material is consumed. To the reaction mixture is added lithium hydroxide (solution in water) and methanol and the resulting solution is stirred for additional time at ambient temperature. The reaction mixture is then concentrated under reduced pressure and the resulting residue is purified by reverse phase chromatography (10-100% MeCN/water with 0.1% ammonium formate) to yield the desired product Compound 5.
 

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