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Chemical Structure| 1246532-96-6 Chemical Structure| 1246532-96-6

Structure of 1246532-96-6

Chemical Structure| 1246532-96-6

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Product Details of [ 1246532-96-6 ]

CAS No. :1246532-96-6
Formula : C16H25N3O3
M.W : 307.39
SMILES Code : O=C(N1CCN(C2=CC=C(N)C(OC)=C2)CC1)OC(C)(C)C
MDL No. :MFCD22192405

Safety of [ 1246532-96-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 1246532-96-6 ]

* 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 [ 1246532-96-6 ]

[ 1246532-96-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1246532-96-6 ]
  • [ 76661-24-0 ]
  • [ 1254783-97-5 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate;tris-(dibenzylideneacetone)dipalladium(0); XPhos; In iso-butanol; at 90℃; for 2.0h; tert-butyl 4-(4-(5-chloro-4-(3-nitrophenoxy)pyrimidin-2-ylamino)-3- methoxyphenyl)piperazine-l-carboxylate A flask was charged with 2,5-dichloro-4-(3- nitrophenoxy)pyrimidine (200mg, 0.7mmol), tert-butyl 4-(4-amino-3- methoxyphenyl)piperazine-l-carboxylate (215mg, 0.7mmol), Pd2(dba)3(64mg, 0.07mmol)), X-Phos (33 mg, 0.07mmol), potassium carbonate (200mg, 1.4mmol) in 2-BuOH (1OmL). The mixture was degased and heated to 9O0C for 2 hours. The slurry was filtrated through celite and washed with ethyl acetate. The concentrated residue was purified by flash chromatography to afford the title compound. MS(M+1): 558.0.
  • 2
  • [ 1246532-96-6 ]
  • [ 1197953-49-3 ]
  • C28H36ClN6O4P [ No CAS ]
YieldReaction ConditionsOperation in experiment
900 mg With palladium diacetate; caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In N,N-dimethyl-formamide; at 110℃; for 1.5h;Microwave irradiation; Inert atmosphere; AP26113 intermediate (2g, 6.3mmol) was added sequentially in a standard microwave reaction tube at room temperature.SIAIS 1197129 (2.4 g, 7.8 mmol), Pd(OAc) 2 (176 mg, 0.78 mmol), Xantphos (810 mg, 1.4 mmol),cesium carbonate (6.4 g, 19.6 mmol), 30 mL DMF, followed by argon exchange, microwave reaction at 110 C for 1.5 h. TLC detection reactionAfter the bundle, the mixture was filtered through silica gel, water-purified, ethyl acetate, washed with water, dried over anhydrous sodium sulfate,Methanol and water gave a reddish brown solid (900 mg) directly to the next step.
With palladium diacetate; caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In N,N-dimethyl-formamide; at 110℃; for 2h;Inert atmosphere; Microwave irradiation; To a solution of <strong>[1197953-49-3]2,5-dichloro-N-(2-(dimethylphosphoryl)phenyl)pyrimidin-4-amine</strong> (2g, 6.3mmol) in DMF (30mL) were added s-2a (2.4g, 7.8mmol)Pd(OAc)2 (176mg, 0.78mmol)Xantphos (810mg, 1.4mmol) and Cs2CO3(6.4g, 19.6mmol) in microwave tube, the solution was purged and refilled with nitrogen three times. Then the mixture was stirred at 110C for 2h in the microwave. After the starting material was consumed, the reaction mixture was filtered through a pad of silica gel and most of the solvent of the filtrate was removed under the reduced pressure. Then the mixture was quenched with water, extracted with ethyl acetate, washed with water and brine, dried over anhydrous Na2SO4. The solvent was evaporated under the reduced pressure and the residue was purified by reverse phase ISCO (C18) to give the title compound s-3a as a brown solid.
 

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