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Chemical Structure| 146751-69-1 Chemical Structure| 146751-69-1

Structure of 146751-69-1

Chemical Structure| 146751-69-1

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Product Details of [ 146751-69-1 ]

CAS No. :146751-69-1
Formula : C3H7Cl2NO
M.W : 144.00
SMILES Code : O=C(Cl)CNC.[H]Cl

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Application In Synthesis of [ 146751-69-1 ]

* 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 [ 146751-69-1 ]

[ 146751-69-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 146751-69-1 ]
  • [ 75747-14-7 ]
  • [ 857402-33-6 ]
YieldReaction ConditionsOperation in experiment
91% 17-Allylaminogeldanamycin (1) (15.1 mg, 0.0258 mmol, 1.0 equiv) was dissolved in 1.5 mL dichloromethane and stirred with a 10% aqueous solution of sodium hydrosulfite (1.5 mL). The deep purple solution turned yellow after 5 min and the mixture was stirred for an additional 25 min. The organic layer was removed via syringe and the aqueous solution was extracted with an additional 0.30 mL dichloromethane. The combined organic solutions were washed with brine (1.0 mL) and then added directly to a solution of the acid chloride hydrochloride (3.7 mg, 0.0258 mmol, 1.0 equiv) in 0.20 mL dichloromethane. The reaction mixture was stirred for 2 h and poured into a separatory funnel with 3.0 mL water. The organic layer was extracted and then washed with additional 2.0 mL water. The combined aqueous layers were lyophilized to yield 5 as a white fluffy powder (15.4 mg, 0.0234 mmol, 91% yield). The material was analyzed by 1H NMR in D20 and LC-MS.
91% Example 12: Preparation of N-Methyl Glycine Co-Salt of the Hydroquinone of 17- AAG[0084] <strong>[75747-14-7]17-AAG</strong> (15.1 mg, 0.0258 mmol, 1.0 equiv) was dissolved in 1.5 niL dichloromethane and stirred with a 10% aqueous solution of sodium hydrosulfite (1.5 rnL). The deep purple solution turned yellow after 5 min and the mixture was stirred for an additional 25 min. The organic layer was removed via syringe and the aqueous solution was extracted with an additional 0.30 mL dichloromethane. The combined organic solutions were washed with brine (1.0 mL) and then added directly to a solution of the acid chloride hydrochloride (3.7 mg, 0.0258 mmol, 1.0 equiv) in 0.20 mL dichloromethane. The reaction mixture was stirred for 2 h and poured into a separatory funnel with 3.0 mL water. The organic layer was extracted and then washed with additional 2.0 mL water. The combined aqueous layers were lyophilized to yield 13 as a white fluffy powder (15.4 mg, 0.0234 mmol, 91% yield). The material was analyzed by 1H NMR in D2O and LC-MS.
 

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