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Chemical Structure| 28721-08-6 Chemical Structure| 28721-08-6

Structure of 28721-08-6

Chemical Structure| 28721-08-6

10-Methoxy-5H-dibenzo[b,f]azepine-5-carbonyl chloride

CAS No.: 28721-08-6

4.5 *For Research Use Only !

Cat. No.: A417622 Purity: 95%

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Product Details of [ 28721-08-6 ]

CAS No. :28721-08-6
Formula : C16H12ClNO2
M.W : 285.73
SMILES Code : O=C(Cl)N1C2=CC=CC=C2C=C(OC)C3=CC=CC=C31
MDL No. :MFCD08460124

Safety of [ 28721-08-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 28721-08-6 ]

* 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 [ 28721-08-6 ]

[ 28721-08-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 28721-08-6 ]
  • [ 28721-09-7 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In methanol; for 2h;Heating / reflux; Step 2. Preparation of 10-Methoxy-5H-dibenz [b, f] azepine-5-carboxamide from 10- Methoxy-5H-dibenz [b, f] azepine-5-carbonyl chloride 100 gm of 10-Methoxy-5H-dibenz [b, f] azepine-5-carbonyl chloride is refluxed in 500 m . methanol. Dry ammonia is-passed into the boiling solution for 2 hours. The methanol is distilled water added and the reaction mixture is cooled to 25-30C and filtered. Yield of 10-Methoxy-5H-dibenz [b, f] azepine-5-carboxamide is 82 g.
With ammonia; In methanol; water; at 50℃; for 1h; The solution is heated to 50 DEG C, 300 ml of 28% aqueous ammonia (2.11 mol) are added dropwise to the homogeneous solution, and the mixture is stirred at 50 DEG C for 1 hour. HPLC monitoring after 1 hour indicates that the reaction is complete, and the solvent is partially distilled off at 40 DEG C under vacuum, down to a residual volume of about 400 ml. The solution at 25 DEG C becomes turbid due to precipitation of 10-methoxy-5H- dibenzo [b, f] azepine-5-carboxamide (IV), and the suspension thus formed is used without further purification in the following step.
 

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