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Chemical Structure| 2736497-38-2 Chemical Structure| 2736497-38-2

Structure of 2736497-38-2

Chemical Structure| 2736497-38-2

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Product Details of [ 2736497-38-2 ]

CAS No. :2736497-38-2
Formula : C14H17ClN2O2S
M.W : 312.81
SMILES Code : O=C(OC)C[C@H](N)C1=CC=C(C2=C(C)N=CS2)C=C1.[H]Cl
English Name :Methyl (S)-3-amino-3-(4-(4-methylthiazol-5-yl)phenyl)propanoate hydrochloride

Safety of [ 2736497-38-2 ]

Application In Synthesis of [ 2736497-38-2 ]

* 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 [ 2736497-38-2 ]

[ 2736497-38-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2316837-29-1 ]
  • [ 2736497-38-2 ]
  • [ 2736497-39-3 ]
YieldReaction ConditionsOperation in experiment
63% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0 - 20℃; for 2h;
56% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 12h; Step 4: To a solution of Intermediate 45-3 (2 g, 6.39 mmol) in DMF (20 mL) wa added DIPEA (5.28 mL, 31.97 mmol,), Intermediate 44 (2.53 g, 7.67 mmol) and HATU (2.92 g, 7.67 mmol) at 20°C. The mixture was stirred at rt for 12 h and then poured into H2O (20 ml) and extracted with EtOAc (3 x 50 mL). The combined organic layers were dried over Na2S04, filtered and concentrated. The crude was purified by HPLC (88:12 to 48:52 H2O (0.09% TFA): CH3CN) to obtain (S)-methyl 3-((2S,4R)-1-((S)-2-(l- fluorocyclopropanecarboxamido)-3,3-dimethylbutanoyl)-4-hydroxy pyrrolidine-2 - carboxamido)-3-(4-(4-methylthiazol-5-yl) phenyl)propanoate (Intermediate 45-4) (2.1 g, 56% yield) as a white solid. LCMS (ESI) m/z 589.4 [M+
56% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 12h; Step 4: To a solution of Intermediate 45-3 (2 g, 6.39 mmol) in DMF (20 mL) wa added DIPEA (5.28 mL, 31.97 mmol,), Intermediate 44 (2.53 g, 7.67 mmol) and HATU (2.92 g, 7.67 mmol) at 20°C. The mixture was stirred at rt for 12 h and then poured into H2O (20 ml) and extracted with EtOAc (3 x 50 mL). The combined organic layers were dried over Na2S04, filtered and concentrated. The crude was purified by HPLC (88:12 to 48:52 H2O (0.09% TFA): CH3CN) to obtain (S)-methyl 3-((2S,4R)-1-((S)-2-(l- fluorocyclopropanecarboxamido)-3,3-dimethylbutanoyl)-4-hydroxy pyrrolidine-2 - carboxamido)-3-(4-(4-methylthiazol-5-yl) phenyl)propanoate (Intermediate 45-4) (2.1 g, 56% yield) as a white solid. LCMS (ESI) m/z 589.4 [M+
With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃;

 

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