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Chemical Structure| 204378-34-7 Chemical Structure| 204378-34-7

Structure of 204378-34-7

Chemical Structure| 204378-34-7

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Product Details of [ 204378-34-7 ]

CAS No. :204378-34-7
Formula : C7H6ClNO3
M.W : 187.58
SMILES Code : O=C(O)C1=NC(OC)=CC(Cl)=C1
MDL No. :MFCD13188726

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Application In Synthesis of [ 204378-34-7 ]

* 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 [ 204378-34-7 ]

[ 204378-34-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 204378-34-7 ]
  • [ 2343-22-8 ]
  • [ 1158970-02-5 ]
YieldReaction ConditionsOperation in experiment
50% With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In N,N-dimethyl-formamide; at 20℃; for 3h; Intermediate 10; 1-[6'-(5-Fluoro-2,3-dihydro-indole-1-carbonyl)-2'-methoxy-3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one; Step 1: (4-Chloro-6-methoxy-pyridin-2-yl)-(5-fluoro-2,3-dihydro-indol-1-yl)-methanone; 550 mg (2.93 mmol) 4-chloro-6-methoxy-pyridine-2-carboxylate, 411 mg (3.00 mmol) <strong>[2343-22-8]5-fluoroindoline</strong>, 1.06 g (3.30 mmol) TBTU and 927 uL (6.60 mmol) triethylamine in 5.00 mL DMF were stirred for 3 h at RT. The reaction mixture was purified by HPLC. The product-containing fractions were combined and evaporated down using the rotary evaporator.Yield: 450 mg (50% of th.)ESI-MS: m/z=307/309 (M+H)+ (CI)Rt (HPLC): 1.7 min (method C)
50% With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In N,N-dimethyl-formamide; at 20℃; for 3h; Intermediate 10(4-chloro-6-methoxy-pyridin-2-yl)-(5-fluoro-2,3-dihydro-indol-1-yl)-methanone 550 mg (2.93 mmol) 4-chloro-6-methoxy-pyridin-2-carboxylic acid, 411 mg (3.00 mmol) <strong>[2343-22-8]5-fluoroindoline</strong>, 1.06 g (3.30 mmol) TBTU and 927 μL (6.60 mmol) triethylamine in 5.00 mL DMF were stirred for 3 h at RT. The reaction mixture was purified by HPLC. The product-containing fractions were combined and evaporated down using the rotary evaporator. Yield: 450 mg (50% of theoretical)ESI-MS: m/z=307/309 (M+H)+ (Cl)Rt(HPLC): 1.7 min (method C)
 

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