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Chemical Structure| 442910-33-0 Chemical Structure| 442910-33-0

Structure of 442910-33-0

Chemical Structure| 442910-33-0

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Product Details of [ 442910-33-0 ]

CAS No. :442910-33-0
Formula : C7H5BrFI
M.W : 314.92
SMILES Code : IC1=CC=C(F)C(CBr)=C1
MDL No. :MFCD18396956

Safety of [ 442910-33-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 442910-33-0 ]

* 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 [ 442910-33-0 ]

[ 442910-33-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 442910-33-0 ]
  • [ 102831-44-7 ]
  • [ 1435479-71-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 1h;Inert atmosphere; 2-tert-Butoxycarbonylamino-2-(2-fluoro-5-iodo-benzyl)-malonic acid diethyl ester (G- 22)A solution of diethyl(Boc-amino)malonate (6.96 g, 25.3 mmol, either commercially available or prepared by conventional Boc-protection of diethylaminomalonate hydrochloride) in DMF (7 ml_) was added dropwise to a 0C suspension of sodium hydride (0.926 g, 23.2 mmol) in DMF (45 ml_) under N2 and then a solution of 2-bromomethyl-1 -fluoro-4-iodo-benzene G-14 (6.62 g, 21 .1 mmol) in DMF (30 ml_) was added to the suspension. The resulting solution was warmed to RT and stirred for 1 h. The reaction was quenched by the addition of water and the mixture was extracted with DCM (3x). The combined organic extracts were washed with brine, dried over Na2S04, filtered and evaporated in vacuo to give the crude product as a white solid that was used further without purification. LC-MS B: tR = 1 .05 min; [M+H]+ = 510.02.
With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 1h;Inert atmosphere; A solution of diethyl(Boc-amino)malonate (6.96 g, 25.3 mmol, either commercially available or prepared by conventional Boc-protection of diethylaminomalonate hydrochloride) in DMF (7 mL) was added dropwise to a 0 C. suspension of sodium hydride (0.926 g, 23.2 mmol) in DMF (45 mL) under N2 and then a solution of 2-bromomethyl-1-fluoro-4-iodo-benzene G-14 (6.62 g, 21.1 mmol) in DMF (30 mL) was added to the suspension. The resulting solution was warmed to RT and stirred for 1 h. The reaction was quenched by the addition of water and the mixture was extracted with DCM (3×). The combined organic extracts were washed with brine, dried over Na2SO4, filtered and evaporated in vacuo to give the crude product as a white solid that was used further without purification. LC-MS B: tR=1.05 min; [M+H]+=510.02
 

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