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Chemical Structure| 1400997-38-7 Chemical Structure| 1400997-38-7

Structure of 1400997-38-7

Chemical Structure| 1400997-38-7

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Product Details of [ 1400997-38-7 ]

CAS No. :1400997-38-7
Formula : C15H19BrFNO3
M.W : 360.22
SMILES Code : O=C(N1CC(C2=CC=C(Br)C(F)=C2)OCC1)OC(C)(C)C
MDL No. :MFCD23703467

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Application In Synthesis of [ 1400997-38-7 ]

* 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 [ 1400997-38-7 ]

[ 1400997-38-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1400997-38-7 ]
  • [ 39268-74-1 ]
  • [ 1400997-42-3 ]
YieldReaction ConditionsOperation in experiment
18% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); tert-butyl XPhos; In 1,4-dioxane; at 120℃; for 16h;Inert atmosphere; EXAMPLE 100(RS)-(5-Ethoxy-pyrimidin-2-yl)-(2-fluoro-4-morpholin-2-yl-phenyl)-aminea) (RS)-2-[4-(5-Ethoxy-pyrimidin-2-ylamino)-3-fluoro-phenyl]-morpholine-4-carboxylic acid tert-butyl esterTo a 10 ml glass vial was added (RS)-2-(4-bromo-3-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (70 mg, Example 96(e)) and <strong>[39268-74-1]5-ethoxy-2-pyrimidinamine</strong> (40.6 mg, CAS 39268-74-1) in dioxane (2 ml). The reaction mixture was purged with argon for 5 min. 2-Di-tert-butylphosphino-2',4',6'-triisopropylbiphenyl (13.6 mg), tris(dibenzylideneacetone)dipalladium(0) (7.12 mg) and sodium tert-butoxide (21.0 mg) were then added. The vial was capped and heated at 120 C. for 16 h. The reaction mixture was then filtered through sintered glass and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (silica gel; gradient: 0% to 50% EtOAc in hexanes) to afford (RS)-2-[4-(5-ethoxy-pyrimidin-2-ylamino)-3-fluoro-phenyl]-morpholine-4-carboxylic acid tert-butyl ester (15 mg, 18%) as a yellow gum. MS (ISP): 441.4 ([M+Na]+), 419.3 ([M+H]+).
18% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); tert-butyl XPhos; In 1,4-dioxane; at 120℃; for 16h;Inert atmosphere; capped vial; To a 10 ml glass vial was added (RS)-2-(4-bromo-3-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (70 mg, Example 96(e)) and <strong>[39268-74-1]5-ethoxy-2-pyrimidinamine</strong> (40.6 mg, CAS 39268-74-1) in dioxane (2 ml). The reaction mixture was purged with argon for 5 min. 2-Di-tert- butylphosphino-2',4',6'-triisopropylbiphenyl (13.6 mg), tris(dibenzylideneacetone)dipalladium(0) (7.12 mg) and sodium tert-butoxide (21.0 mg) were then added. The vial was capped and heated at 120 C for 16 h. The reaction mixture was then filtered through sintered glass and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (silica gel; gradient: 0% to 50% EtOAc in hexanes) to afford (RS)-2-[4-(5-ethoxy-pyrimidin-2-ylamino)-3- fluoro-phenyl]-morpholine-4-carboxylic acid tert-butyl ester (15 mg, 18%) as a yellow gum. MS (ISP): 441.4 ([M+Na]+), 419.3 ([M+H]+).
  • 2
  • [ 1003879-02-4 ]
  • [ 1400997-38-7 ]
 

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