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Chemical Structure| 857651-11-7 Chemical Structure| 857651-11-7

Structure of 857651-11-7

Chemical Structure| 857651-11-7

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Product Details of [ 857651-11-7 ]

CAS No. :857651-11-7
Formula : C5H12ClNO
M.W : 137.61
SMILES Code : O[C@H]1CN[C@H](C)C1.[H]Cl
MDL No. :MFCD27920656

Safety of [ 857651-11-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 857651-11-7 ]

* 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 [ 857651-11-7 ]

[ 857651-11-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 857651-11-7 ]
  • [ 17794-48-8 ]
  • [ 857651-12-8 ]
YieldReaction ConditionsOperation in experiment
81% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 4h; (3R,5R)-5-Methylpyrrolidin-3-ol hydrochloride (1.80 g, 13 mmol) was dissolved in dichloromethane (50 mL) and diisopropylethylamine (2.1 mL, 12.0 mmol) under nitrogen. (3-Trifluoromethyl-benzoylamino)-acetic acid (2.93 g, 11.85 mmol) was added followed by EDC (3.41 g, 17.8 mmol) and the mixture was stirred at room temperature for four hours. The mixture was diluted with NH4Cl/H2O and extracted twice with ethyl acetate. The combined extracts were washed with NaHCO3/H2O and brine, dried over MgSO4, filtered and concentrated to give a dark orange oil. Chromatography on silica gel eluting with ethyl acetate to 5% methanol/ethyl acetate gave the coupled product as a pale orange solid, 3.19 g (81%, 2 steps). LC/MS (M+H)+ m/z=331.1. 1H NMR (CDCl3, major rotamer) delta 8.12 (s, 1H), 8.01 (d, 1H), 7.76 (d, 1H), 7.57 (t, 1H), 7.50 (m, 1H), 4.56 (m, 1H), 4.34 (m, 1H), 4.23 (m, 1H), 4.11 (m, 1H), 3.61 (dd, 1H), 3.51 (d, 1H), 2.71 (d, 1H), 2.17 (m, 1H), 1.81 (m, 1H), 1.32 (d, 3H).
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 4h;Inert atmosphere; Step GN-{2-[(2f?,4f?)-4-Hydroxy-2-methylpyrrolidin-1 -yl]-2-oxoethyl}-3-(trifluoro- methyl)benzamide. (3f?,5f?)-5-Methylpyrrolidin-3-ol hydrochloride (1.80 g) was dissolved in dichloromethane (50 mL) and diisopropylethylamine (2.1 mL, 12.0 mmol) under nitrogen. (3- Trifluoromethyl-benzoylamino)-acetic acid (2.93 g, 1 1.85 mmol) was added followed by EDC (3.41 g, 17.8 mmol) and the mixture was stirred at room temperature for four hours. The mixture was diluted with NH4CI/H20 and extracted twice with ethyl acetate. The combined extracts were washed with NaHC03/H20 and brine, dried over MgS04, filtered and concentrated to give a dark orange oil. Chromatography on silica gel eluting with ethyl acetate to 5% methanol/ethyl acetate gave the coupled product as a pale orange solid, 3.19 g (81 %, 2 steps). LC/MS (M+H)+ m/z = 331 .1. 1H NMR (CDCI3, major rotamer) delta 8.12 (s, 1 H), 8.01 (d, 1 H), 7.76 (d, 1 H), 7.57 (t, 1 H), 7.50 (m, 1 H), 4.56 (m, 1 H), 4.34 (m, 1 H), 4.23 (m, 1 H), 4.1 1 (m, 1 H), 3.61 (dd, 1 H), 3.51 (d, 1 H), 2.71 (d, 1 H), 2.17 (m, 1 H), 1.81 (m, 1 H), 1.32 (d, 3H).
 

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