1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

Base Information

Chemical Name:1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one
CAS No.:1628074-91-8
Molecular Formula:C₃₆H₃₁N₃O₃
Molecular Weight:553.66
Hs Code.:

Synonyms:1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

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Chemical Property of 1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

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Technology Process of 1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

There total 1 articles about 1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 118-12-7
1,3,3-Trimethyl-2-methyleneindoline

: 937-31-5
(4-Nitrophenyl)acetylene

: 122100-99-6
3-phenyl-propynoic acid (2-iodo-phenyl)-methyl-amide

: 1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

: 1628074-91-8
1-methyl-3-(3-(4-nitrophenyl)-1-phenyl-2-(1,3,3-trimethylindolin-2-ylidene)but-3-en-1-ylidene)indolin-2-one

Guidance literature:: (4-Nitrophenyl)acetylene; 3-phenyl-propynoic acid (2-iodo-phenyl)-methyl-amide; With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 16h; Inert atmosphere;

1,3,3-Trimethyl-2-methyleneindoline; In tetrahydrofuran; ethanol; at 80 ℃; for 48h; Overall yield = 91 %; Overall yield = 504 mg; Optical yield = 4 %de; diastereoselective reaction; Inert atmosphere; Sealed tube;
DOI:10.3762/bjoc.10.51