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Chemical Structure| 1374215-03-8 Chemical Structure| 1374215-03-8

Structure of 1374215-03-8

Chemical Structure| 1374215-03-8

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Product Details of [ 1374215-03-8 ]

CAS No. :1374215-03-8
Formula : C9H9ClN2O2
M.W : 212.63
SMILES Code : O=C(O)C1=CN=C(Cl)C=C1NC2CC2
MDL No. :MFCD24502869

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Application In Synthesis of [ 1374215-03-8 ]

* 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 [ 1374215-03-8 ]

[ 1374215-03-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 233764-32-4 ]
  • [ 1374215-03-8 ]
  • [ 1610021-15-2 ]
YieldReaction ConditionsOperation in experiment
63% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20℃; for 3h; [00202j Step 3: To a stirred solution of 6-chloro-4-(cyclopropylamino)nicotinic acid(0.30 g, 1.4 mmol) in DMF (5mL) was added HATU (0.644 g, 1.7 mmol), DIPEA (0.74mL, 4.23 mmol) and (1R,4R)-<strong>[233764-32-4]4-amino-1-methylcyclohexanol</strong> (0.219 g, 1.693 mmol). The mixture was stirred for 3 hours at room temperature. The DMF was evaporated from the reaction mixture and the residue was partitioned with water and EtOAc. The organic layer was washed with cold water (3 times). The organic layer was dried over Na2504and concentrated under vacuum to get crude compound which was then purified by flash column chromatography (10% MeOH/DCM) to afford 6-chloro-4-(cyclopropylamino)-N- (4-hydroxy-4-methylcyclohexyl)nicotinamide (310 mg, 63% yield). LCMS m/z 324.2 (M+H).
63% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20℃; for 3h; [00254j To a stirred solution of 6-chloro-4-(cyclopropylamino)nicotinic acid (0.30 g,1.4 mmol) in DMF (5mL) was added HATU (0.644 g, 1.7 mmol), DIPEA (0.74 mL, 4.23 mmol) and (1R,4R)-<strong>[233764-32-4]4-amino-1-methylcyclohexanol</strong> (0.2 19 g, 1.693 mmol). The mixture was stirred for 3 hours at room temperature. The DMF was evaporated from the reaction mixture and the residue was partitioned with water and EtOAc. The organic layer waswashed with cold water (3 times). The organic layer was dried over Na2SO4 andconcentrated under vacuum to get crude compound which was then purified by flashcolumn chromatography (10% MeOH/DCM) to afford 6-chloro-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide (310 mg, 63% yield). LCMS m/z 324.2 (M+H).
 

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