84764-41-0

Usage

Molecular Structure

A complex structure consisting of an isoindole ring and a 1,3-dione functional group.

Side Chain

A 2-(2-methyl-1,3-dioxolan-2-yl)ethyl side chain attached to the isoindole ring.

Isoindole Ring

A fused bicyclic ring system with one six-membered benzene ring and one five-membered nitrogen-containing ring.

1,3-Dione Functional Group

A functional group consisting of two carbonyl groups (C=O) located at the 1 and 3 positions of the isoindole ring.

2-Methyl-1,3-Dioxolan-2-Yl Group

A 1,3-dioxolan ring with a methyl group attached to the 2 position.

Ethyl Side Chain

A two-carbon alkyl chain (C2H5) connected to the 2-methyl-1,3-dioxolan-2-yl group.

Potential Applications

Possible uses in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties.

Further Research

Necessary to fully understand the characteristics and potential uses of this chemical compound.

Upstream product

• 136918-14-4 phthalimide 
• 1074-82-4 potassium phtalimide 
• 3783-77-5 N-(3-oxobutyl)phthalimide 
• 107-21-1 ethylene glycol 

Downstream Products

• 62240-37-3 2-(2-methyl-1,3-dioxolane-2-yl)ethan-1-amine 
• 138489-32-4 C₃₄H₄₃NO₄Se 
• 138489-31-3 C₃₄H₅₃NO₄SSi 
• 138489-36-8 C₂₉H₃₆ClNO₄ 
• 138489-35-7 C₂₉H₃₇NO₅ 
• 104115-60-8 C₃₀H₄₁NO₅ 
• 138489-29-9 C₃₁H₄₅NO₄S 
• 138489-27-7 (1''R+S,7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-(1'',5''-dimethyl-3''-oxohexyl)-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-one 
• 138489-37-9 C₃₀H₃₉NO₄ 
• 104115-49-3 (1''R+S,7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-(1''-methyl-3''-oxobutyl)-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-thione 
• 138602-83-2 (3aS^*,12α,12aα,12bβ)-(+/-)-2,3,6,7,11,12,12a,12b-Octahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 104115-52-8 (3aS^*,8aα,12aα,12bβ)-(+/-)-2,3,6,7,8a,9,12a,12b-Octahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 138602-84-3 (3aS^*,8aα,12α,12aα,12bβ)-(+/-)-Decahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 138489-28-8 (7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>thioxolan>-6(7H)-thione 

Relevant academic research and scientific papers

Highly Regioselective 5-endo-tet Cyclization of 3,4-Epoxy Amines into 3-Hydroxypyrrolidines Catalyzed by La(OTf)3

Highly regioselective intramolecular aminolysis of 3,4-epoxy amines has been achieved. Key features of this reaction are (1) chemoselective activation of epoxides in the presence of unprotected aliphatic amines in the same molecules by a La(OTf)3 catalyst and (2) excellent regioselectivity for anti-Baldwin 5-endo-tet cyclization. This reaction affords 3-hydroxy-2-alkylpyrrolidines stereospecifically in high yields. DFT calculations revealed that the regioselectivity might be attributed to distortion energies of epoxy amine substrates. The use of this reaction was demonstrated by the first enantioselective synthesis of an antispasmodic agent prifinium bromide.

Synthesis method of 5-benzyl-2-tert-butyl-8-oxo-2,5-diazaspiro[3,5]nonanyl-2,5-dicarboxylic acid

The invention relates to a synthesis method of 5-benzyl-2-tert-butyl-8-oxo-2,5-diazaspiro[3,5]nonanyl-2,5-dicarboxylic acid. The technical problem of no industrial synthesis routes is mainly solved. The method comprises the following steps: carrying out a

New efficient synthesis of pyrido[2,3-c] and pyrido[3,2-c]coumarin derivatives

Various substituted pyrido[2,3-c] and pyrido[3,2-c]coumarins are efficiently prepared in three steps from 3- and 4-hydroxycoumarins, respectively and protected β-aminoketones.

Benzomorphan-related Compounds. Part 21. Synthesis of 7,8-Benzomorphans via 2-Aryl-4-piperidones

A new synthesis of 1,2,3,4,5,6-hexahydro-1,5-methano-2-benzazocines (7,8-benzomorphans) based on the acid-catalysed cyclization of 2-arylpiperidine-4-carboxylic acids is reported.The required carboxylic acids were prepared from 2-aryl-4-piperidones, by re