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Chemical Structure| 1338243-88-1 Chemical Structure| 1338243-88-1

Structure of 1338243-88-1

Chemical Structure| 1338243-88-1

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Product Details of [ 1338243-88-1 ]

CAS No. :1338243-88-1
Formula : C16H21NO4
M.W : 291.34
SMILES Code : O=C(OC)C1=CC=C(C2(NC(OC(C)(C)C)=O)CC2)C=C1
MDL No. :MFCD24467647
InChI Key :AAHYXLNOQOLLSL-UHFFFAOYSA-N
Pubchem ID :58458632

Safety of [ 1338243-88-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1338243-88-1 ]

* 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 [ 1338243-88-1 ]

[ 1338243-88-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 1338243-88-1 ]
  • [ 1014645-87-4 ]
YieldReaction ConditionsOperation in experiment
5.3 g With hydrogenchloride In ethyl acetate at 20℃; To a cooled solution of methyl 4-(1-((tert-butoxycarbonyl)amino)cyclopropyl)benzoate (D5) (7.4 g, 25.4 mmol) in ethyl acetate (10 ml) HCl (g)/ethyl acetate (4N, 50 ml) was added the mixture was stirred at room temperature overnight. Evaporated the solvent, the residue was washed with petroleum ether to afford the title compound (D7) (5.3 g) as a white solid.
References: [1] Patent: WO2012/76063, 2012, A1, . Location in patent: Page/Page column 38-39.
[2] Patent: US2013/261100, 2013, A1, . Location in patent: Paragraph 0273-0275.
 

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