3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

Base Information

Chemical Name:3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine
CAS No.:1346445-99-5
Molecular Formula:C₁₅H₁₅N₅O
Molecular Weight:281.317
Hs Code.:

Synonyms:3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

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Technology Process of 3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

There total 2 articles about 3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine 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: 95.0%

: 141-97-9
ethyl acetoacetate

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1346445-99-5
3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

Guidance literature:: With triethanolamine; ammonium acetate; sodium acetate; hydrazine hydrate; for 0.05h; Microwave irradiation;
DOI:10.1007/s13738-021-02178-z

Reference yield: 91.0%

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 105-45-3
acetoacetic acid methyl ester

: 1346445-99-5
3,5-dimethyl-4-(4-hydroxyphenyl)-1,4,7,8-tetrahydrodipyrazolo[3,4-b;4’,3’-e]pyridine

Guidance literature:: With urease covalently immobilized on cotton-derived nanocellulose-dialdehyde; hydrazine hydrate; urea; In water; at 70 ℃; for 1.33333h; Green chemistry; Enzymatic reaction;
DOI:10.1039/c9ra05240b