65222-35-7 Usage
Uses
Used in Medicinal Chemistry:
N,N-diethyl-N'-(6-methyl-5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolin-10-yl)propane-1,3-diamine is used as a building block or intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features and potential for forming stable complexes with biological targets.
Used in Organic Synthesis:
In the field of organic synthesis, N,N-diethyl-N'-(6-methyl-5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolin-10-yl)propane-1,3-diamine serves as a versatile reagent or precursor for the creation of a wide range of organic molecules, including those with potential applications in materials science and specialty chemicals.
Used in Pharmacology Research:
Check Digit Verification of cas no
The CAS Registry Mumber 65222-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65222-35:
(7*6)+(6*5)+(5*2)+(4*2)+(3*2)+(2*3)+(1*5)=107
107 % 10 = 7
So 65222-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H27N5/c1-4-27(5-2)12-6-9-24-22-18-13-17-19-14-23-10-8-20(19)26-21(17)15(3)16(18)7-11-25-22/h7-8,10-11,13-14,26H,4-6,9,12H2,1-3H3,(H,24,25)
65222-35-7Relevant academic research and scientific papers
Industrial synthesis in mass production. Ellipticine. II. The elaboration of a new approach to GH-pyrido[4,3:b]carbazoles and analogs. B. The recovery of tetracyclic structures
Dormoy,Heymes
, p. 2915 - 2938 (2007/10/02)
Total synthesis of modified ellipticines 1c and 1f is described from 2-chloronicotinic acid and respectively 5-methoxy-indole and 5-azaindole in 11 to 13 steps with overall yields of 11% and 18%. With respect to the numerous synthesis described in the literature, the originality of this approach resides above all in the formation of ring C in basic medium, such conditions being dictated by the presence of the pyridine A ring in the case of 1f. Both synthesis have been extrapolated to produce several kilograms of final product. The second part deals with the elaboration of tetracyclic structures from precursors.
Process for the preparation of isoquinoline derivatives
-
, (2008/06/13)
The subject of the present invention is a process for the preparation of isoquinoline derivatives in four steps wherein use is made as synthetic intermediates of organo-lithium compounds or related compounds.
