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Chemical Structure| 1221793-42-5 Chemical Structure| 1221793-42-5

Structure of 1221793-42-5

Chemical Structure| 1221793-42-5

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Product Details of [ 1221793-42-5 ]

CAS No. :1221793-42-5
Formula : C11H17F2NO4
M.W : 265.25
SMILES Code : O=C([C@H]1N(C(OC(C)(C)C)=O)CCC(F)(F)C1)O
MDL No. :MFCD03094869
InChI Key :BEYLYGCFFXJNQM-ZETCQYMHSA-N
Pubchem ID :49759774

Safety of [ 1221793-42-5 ]

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

Application In Synthesis of [ 1221793-42-5 ]

* 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.

  • Upstream synthesis route of [ 1221793-42-5 ]

[ 1221793-42-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 1352342-07-4 ]
  • [ 1221793-42-5 ]
YieldReaction ConditionsOperation in experiment
98%
Stage #1: With water; potassium hydroxide In tetrahydrofuran; methanol at 20℃; for 2.5 h;
Stage #2: With hydrogenchloride In water
A solution of compound 2 (1.526 g, 5.462 mmol) in THF (11 mL), methanol (11 mL), and 1 N KOH (11 mL, 11 mmol) was stirred at rt for 1.5 h and then additional 1 N KOH (5.5 mL, 5.5 mmol) was added. After 1 h, the mixture was concentrated to a half volume and diluted with water before washing with ether (x 1). The aqueous solution was acidified with 1 N HCI (20 mL) and the product was extracted with ethyl acetate (x 2). The extracts were washed with brine (x 1), combined, dried (Na2SO4), and concentrated to obtain compound 3 (1.429 g, 98percent). MS [M-H]" = 264.2
93% With potassium hydroxide In tetrahydrofuran; methanol; water at 20℃; To the reaction flask was added (S) -1-tert-butyl-2-methyl-4,4-difluoropiperidine-1,2-dicarboxylate 10c (2.6 g, 9.3 mmol)Potassium hydroxide (1.5 g, 26.8 mmol), methanol (18 mL),Tetrahydrofuran (18 mL) and water (18 mL),Stir overnight at room temperature.The reaction solution was cooled in vacuo to adjust the pH of the reaction solution to pH 2-3, concentrated under reduced pressure, and each was extracted with ethyl acetate and water (50 mL). The aqueous phase was extracted with ethyl acetate (30 mL x 2) The organic phases were combined, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and purified by silica gel column chromatography (petroleum ether / ethyl acetate (v / v) = 5: 1-3: 1)To give a pale yellow oil1- (tert-butoxycarbonyl) -4,4-difluoropiperidine-2-carboxylic acid for 10d (2.3 g, yield 93percent).
References: [1] Patent: WO2011/156610, 2011, A2, . Location in patent: Page/Page column 102.
[2] Patent: CN106928127, 2017, A, . Location in patent: Paragraph 0232; 0243; 0244; 0245; 0246; 0247.
[3] Patent: WO2015/5901, 2015, A1, . Location in patent: Page/Page column 528; 529.
 

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