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Structure of 25654-52-8

Chemical Structure| 25654-52-8

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Product Details of [ 25654-52-8 ]

CAS No. :25654-52-8
Formula : C12H13NO4
M.W : 235.24
SMILES Code : O=C([C@H]1N(C(OCC2=CC=CC=C2)=O)CC1)O
MDL No. :MFCD09954924

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Application In Synthesis of [ 25654-52-8 ]

* 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 [ 25654-52-8 ]

[ 25654-52-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 125178-42-9 ]
  • [ 2133-34-8 ]
  • [ 25654-52-8 ]
  • 2
  • [ 501-53-1 ]
  • [ 2133-34-8 ]
  • [ 25654-52-8 ]
YieldReaction ConditionsOperation in experiment
90.2% With sodium hydroxide; In water; at 0 - 20℃; To a mixture of (5)-azetidine-2-carboxylic acid (1.0 g, 9.89 mmol) in aqueous NaOH solution (2.5 mL, 10 mmol, 4M) was added aqueous sodium hydroxide solution (3.0 mL, 12 mmol, 4 M) drop-wise at 0C, followed by drop-wise addition of benzylcarbonochloridate (1.53 mL, 10.88 mmol). After the addition was complete, the reaction was stirred at room temperature overnight. The reaction mixture was then washed with diethyl ether (30 mL), and the water layer was acidified with dilute hydrochloric acid (1M). The water layer was then extracted with ethyl acetate (30 mL x 3), and the combined ethyl acetate extracts were dried over Na2SO4, filtered and concentrated to give (S)-1-((benzyloxy)carbonyl)azetidine-2-carboxylic acid (2.1 g, 90.2% yield) as a colorless oil. LC-MS: m/z = 236 [M+Hf?, ee> 99% (CHIRALPAK AS-H, 15% ethanol / hexane).
53% To a solution of <strong>[2133-34-8]L-azetidine-2-carboxylic acid</strong> (101.1 mg, 1 mmol) in 2N aqueousNaOH (0.675 ml) is added benzylchloroformiate (169 ul, 204.7 mg, 1.2 eq.) and theresulting mixture is stirred at rt for 2 h. The aqueous phase is washed once with EtiO.The aqueous solution is set to pH=2 with a concentrated aqueous HCI solution and thensaturated with solid Na2SO4. It is extracted three times with AcOEt. The combinedorganic phase is dried over Na2SO4. The solvents are evaporated under a stream of airand the crude oil dried under high vacuum overnight, yielding the title compound (126mg) in 53% as a colourless oil: fa = 0.76 min (LC-3), ESI-MS (pos.): m/z 277.16[M+Naf; ^-NMR (CDC13): 5 (ppm) 2.53 (bs, 2H, C^CHaN), 4.01 (t, 2H, CJJbN),4.82 (t, 1 H, CHC02H), 5.15 (s, 2H, OCtfcPh), 7.35 (s, 5 H, Harom.).
In water; N,N-dimethyl-formamide; at 0 - 20℃; Example 301 (S)-2-[4-(4-Cyclopropylcarbamoyl-phenyl)-thiazol-2-ylcarbamoyl]-azetidine-1-carboxylic acid benzyl ester (Compound 5301) (S)-Azetidine-1,2-dicarboxylic acid 1-benzyl ester (S)-Azetidine-2-carboxylic acid (250.4 mg, 2.5 mmol) was dissolved in DMF (15 mL) and distilled water (6 mL). The solution was cooled to 0 C., and DIEA (645 muL, 3.7 mmol) was added followed by benzyl chloroformate (530 muL, 3.7 mmol). The reaction was stirred at 0 C. and allowed to warm to ambient temperature overnight. The reaction was filtered and purified by reverse phase HPLC to give the desired product.
 

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