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Chemical Structure| 69875-54-3 Chemical Structure| 69875-54-3

Structure of 69875-54-3

Chemical Structure| 69875-54-3

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Product Details of [ 69875-54-3 ]

CAS No. :69875-54-3
Formula : C10H4Cl2N2
M.W : 223.06
SMILES Code : N#CC1=C(Cl)C2=CC=CC=C2N=C1Cl
MDL No. :MFCD00206427

Safety of [ 69875-54-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 69875-54-3 ]

* 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 [ 69875-54-3 ]

[ 69875-54-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 69875-54-3 ]
  • [ 680210-85-9 ]
YieldReaction ConditionsOperation in experiment
94% With ammonium acetate; acetic acid; at 140℃; for 4h; Ammonium acetate (2.1 g, 27 mmol) was added to a suspension of Compound 114 (6.0 g, 27 mmol) in glacial acetic acid and heated at 140 C for 4 h. The solution was cooled and poured into ice water. The solids formed were filtered, washed by water, and dried under vacuum to yield 5.2 g (94%) of white solids. M. P. 302C. 1H NMR (DMSO-DS) : d 1H-NMR (DMSO-d6): 7. 4 (m, 2H), 7.79 (T, J= 7.6 Hz, 1H), 7.96 (d, J= 8. 0 Hz, 1H), ; EIMS : 205 (M+H).
77% With ammonium acetate; acetic acid; at 140℃; for 4h; 2,4-dichloroquinoline-3-carbonitrile (Example 72a) (0.95 g, 4.26 mmol) and ammonium acetate (0.36 g, 4.67 mmol) were heated in acetic acid (20 mL) at 140 C. for 4 hours, then cooled to room temperature. The reaction was poured into ice water (400 mL), and the resultant precipitate was collected by filtration to give 4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.668 g, 77%) as a light yellow solid. M.p.: >250 C. 1H NMR (400 MHz, DMSO-d6) delta 7.42 (m, 2H), 7.79 (m, 1H), 7.96 (d, J=8.4 Hz, 1H), 12.72 (s, 1H). MS 205 (MH-).
With water; trifluoroacetic acid; at 100℃; for 1h; 4-chloro-2-oxo-L2-dihvdroquinoline-3-carbonitrile (1-5) In a round-bottomed flask, 2,4-dichloroquinoline-3-carbonitrile (1-4) (15g, 67.2mmol), was dissolved in 40 ml of a 4: 1 mixture of TFA and H20. The reaction mixture was heated to 100 C for 1 hour, then allowed to cool and poured into methanol. The precipitate was filtered off and dried to give 4-chloro-2-oxo-l,2-dihydroquinoline-3-carbonitrile (1-4) HRMS (M+H)+: observed = 205.1, calculated = 205.6
With trifluoroacetic acid; In water; at 100℃; for 1h; In a round-bottomed flask, 2,4-dichloroquinoline-3-carbonitrile (1-4) (15g, 67.2mmol), was dissolved in 40 ml of a 4: 1 mixture of TFA and H20. The reaction mixture was heated to 100 C for 1 hour, then allowed to cool and poured into methanol. The precipitate was filtered off and dried to give 4-chloro-2-oxo-l,2-dihydroquinoline-3-carbonitrile (1-4) HRMS (M+H)+: observed = 205.1, calculated = 205.6
With trifluoroacetic acid; In water; at 100℃; for 1h; In a round-bottomed flask, 2,4-dichloroquinoline-3 -carbonitrile (1-4) (1 5g,67.2mmol), was dissolved in 40 ml of a 4:1 mixture of TFA and H20. The reaction mixture was heated to 100C for 1 hour, then allowed to cool and poured into methanol. The precipitate was filtered off and dried to give 4-chloro-2-oxo- 1 ,2-dihydroquinoline-3 -carbonitrile (1-4) HRMS(M+H): observed = 205.1, calculated = 205.6

 

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