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Chemical Structure| 173459-03-5 Chemical Structure| 173459-03-5

Structure of 173459-03-5

Chemical Structure| 173459-03-5

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Product Details of [ 173459-03-5 ]

CAS No. :173459-03-5
Formula : C13H10ClN3O
M.W : 259.69
SMILES Code : COC1=CC=C(C2=CC3=C(Cl)N=CN=C3N2)C=C1
MDL No. :MFCD20267237

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Application In Synthesis of [ 173459-03-5 ]

* 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.

  • Downstream synthetic route of [ 173459-03-5 ]

[ 173459-03-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 173459-03-5 ]
  • [ 15996-84-6 ]
  • [ 1350639-68-7 ]
YieldReaction ConditionsOperation in experiment
75% In butan-1-ol; at 145℃; for 24h;Inert atmosphere; General procedure: The following is representative: 4-chloro-6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine (7a) (275 mg, 1.06 mmol) and (R)-1-phenylethanamine (0.44 mL, ∼3.5 mmol) were added to a dry round bottle flask containing 1-butanol (3.5 mL) under argon atmosphere. The mixture was heated at 145 C for 24 h. The precipitate formed upon cooling to rt. was isolated by filtration, washed with diethyl ether (25 mL) and dried resulting in a solid.
In butan-1-ol; at 145℃; General procedure: Compound 1a-d or 54 (1 mmol) was mixed with the selected amine, 2-25, (3 mmol) and n-butanol (5 ml) and agitated at145 C for 14-24 h. Then the mixture was cooled to 22 C, dilutedwith water (15 ml) and ethyl acetate (40 ml). After phase separation,the water phase was back extracted with more ethyl acetate(2 10 ml). The combined organic phases were washed with brine(10 ml), dried over anhydrous Na2SO4, filtered and concentrated invacuo, before the crude mixture was purified as specified for eachindividual compound
In butan-1-ol; at 145℃; for 24h;Inert atmosphere; General procedure: The following is representative: 4-chloro-6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine (14) (275 mg, 1.06 mmol) and (S)-1-phenylethanamine ((S)-19i) (0.44 mL, ∼3.5 mmol) were added to a dry round bottle flask containing 1-butanol (3.5 mL) under argon atmosphere. The mixture was heated at 145 C for 24 h. The precipitate formed upon cooling to rt. was isolated by filtration, washed with diethyl ether (25 mL) and dried resulting in a solid.
  • 2
  • [ 173459-03-5 ]
  • [ 15996-84-6 ]
  • [ 1350639-83-6 ]
  • 3
  • [ 173459-03-5 ]
  • [ 68285-27-8 ]
  • C21H19FN4O [ No CAS ]
YieldReaction ConditionsOperation in experiment
In butan-1-ol; at 145℃; for 24h;Inert atmosphere; General procedure: The following is representative: 4-chloro-6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine (14) (275 mg, 1.06 mmol) and (S)-1-phenylethanamine ((S)-19i) (0.44 mL, ?3.5 mmol) were added to a dry round bottle flask containing 1-butanol (3.5 mL) under argon atmosphere. The mixture was heated at 145 C for 24 h. The precipitate formed upon cooling to rt. was isolated by filtration, washed with diethyl ether (25 mL) and dried resulting in a solid.
 

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