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Chemical Structure| 569660-89-5 Chemical Structure| 569660-89-5

Structure of 569660-89-5

Chemical Structure| 569660-89-5

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Product Details of [ 569660-89-5 ]

CAS No. :569660-89-5
Formula : C9H16BrNO2
M.W : 250.13
SMILES Code : O=C(N1C[C@@H](Br)CC1)OC(C)(C)C
MDL No. :MFCD17214728
InChI Key :QJTKPXFJOXKUEY-ZETCQYMHSA-N
Pubchem ID :34179480

Safety of [ 569660-89-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335-H412
Precautionary Statements:P261-P264-P270-P271-P273-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 569660-89-5 ]

* 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 [ 569660-89-5 ]

[ 569660-89-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109431-87-0 ]
  • [ 569660-89-5 ]
YieldReaction ConditionsOperation in experiment
100% With carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; at 5℃; for 0.0833333h; To a 100 mL round bottom flask was added (R)-(-)-N-Boc-3-pyrrolidinol (1.5 g) under an argon atmosphere. CBr4 (1.5 g) was then added followed by dry THF (50 mL) and the mixture was cooled to 5 C. PPh3 was then added over 5 min and the progress was followed by TLC. The solid was removed by filtration and washed with ether. The filtrate was concentrated and purified by column chromatography eluting with 1:3 EtOAc:Hx. Yield: 2.3 g (>100%, used without further purification). 1H-NMR (CDCl3) δ 4.48 (br s, 1H), 3.82-3.65 (m, 2H), 3.62-3.46 (m, 2H), 2.38-2-18 (m, 2H), 1.46 (s, 9H).
90% With carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; at 60℃; for 1h; Example 8; (R)-N-(2-methoxybenzyl)-1-(1-(2-(methylamino)ethyl)pyrrolidin-3-yl)-3-(trifluoromethyl)-1 H- pyrazole-5-carboxamide (78); <n="77"/>Step 1 (S)-tert-butyl 3-bromopyrrolidine-i-carboxylate (72); [0251] To a stirred solution of N-Boc-(R)-3-hydroxypyrrolidine (0 936 g, 5 mmol) in THF (25 ml_) was added carbon tetrabromide (2 487 g, 7 50 mmol) followed by triphenylphosphine(1 967 g, 7 50 mmol) The resulting suspension was allowed to stir at 60 0C for 1 h Insoluble material was filtered, and concentrated The residue was purified by silica gel column chromatography with a gradient of EtOAc (5-30%) in hexanes to afford 72 (1 12 g, 90%) as a colorless oil LRMS (ESI) calc 249 0, found 271 9 (MNa)+
 

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