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Chemical Structure| 364385-54-6 Chemical Structure| 364385-54-6

Structure of 364385-54-6

Chemical Structure| 364385-54-6

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Product Details of [ 364385-54-6 ]

CAS No. :364385-54-6
Formula : C11H22N2O2
M.W : 214.30
SMILES Code : O=C(OC(C)(C)C)N[C@H]1[C@@H](N)CCCC1
MDL No. :MFCD09952106
InChI Key :AKVIZYGPJIWKOS-DTWKUNHWSA-N
Pubchem ID :1514392

Safety of [ 364385-54-6 ]

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

Application In Synthesis of [ 364385-54-6 ]

* 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 [ 364385-54-6 ]

[ 364385-54-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 105763-77-7 ]
  • [ 364385-54-6 ]
  • [ 364386-47-0 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; water; Step 1 (1R,2S)-N-tert-Butoxycarbonyl-2-(2-chloro-6-methoxyquinazolin-4-yl)aminocyclohexylamine A solution of 710 mg of <strong>[105763-77-7]2,4-dichloro-6-methoxyquinazoline</strong> in 20 mL of methylene chloride was combined with 471 mg of triethylamine and 750 mg of (1S,2R)-2-tert-butoxycarbonylaminocyclohexylamine, and stirred at room temperature for 48 hours. After concentrating, the mixture was combined with water, extracted with methylene chloride, and dried. After solvent was distilled off, the residue was purified by column chromatography on silica gel (chloroform:methanol 20:1) to obtain 1.20 g of the desirable compound.
 

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