6H-Pyrrolo[3,4-b]pyridine-6-acetic acid, 4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-, 1,1-dimethylethyl ester, (4R)-

Base Information

Chemical Name:6H-Pyrrolo[3,4-b]pyridine-6-acetic acid, 4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-, 1,1-dimethylethyl ester, (4R)-
CAS No.:915731-60-1
Molecular Formula:C₂₁H₂₂Cl₂N₂O₄
Molecular Weight:437.323
Hs Code.:

6H-Pyrrolo[3,4-b]pyridine-6-acetic acid,
4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-,
1,1-dimethylethyl ester, (4R)-

Synonyms:

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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 6H-Pyrrolo[3,4-b]pyridine-6-acetic acid, 4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-, 1,1-dimethylethyl ester, (4R)-

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Technology Process of 6H-Pyrrolo[3,4-b]pyridine-6-acetic acid, 4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-, 1,1-dimethylethyl ester, (4R)-

There total 8 articles about 6H-Pyrrolo[3,4-b]pyridine-6-acetic acid, 4-(2,4-dichlorophenyl)-5,7-dihydro-3-(hydroxymethyl)-2-methyl-5-oxo-, 1,1-dimethylethyl ester, (4R)- 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:

: 1454705-52-2
tert-butyl 2-(3-(chlorocarbonyl)-4-(2,4-dichlorophenyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)acetate

: 915297-06-2,915731-60-1,915731-61-2
tert-butyl 2-(4-(2,4-dichlorophenyl)-3-(hydroxymethyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)acetate

Guidance literature:: tert-butyl 2-(3-(chlorocarbonyl)-4-(2,4-dichlorophenyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)acetate; With lithium tri-t-butoxyaluminum hydride; In tetrahydrofuran; at 0 ℃; for 0.416667h;

With water; In tetrahydrofuran;

Reference yield:

: 915296-79-6
(Z)-ethyl 4-chloro-2-(2,4-dichlorobenzylidene)-3-oxobutanoate

: 915297-06-2,915731-60-1,915731-61-2
tert-butyl 2-(4-(2,4-dichlorophenyl)-3-(hydroxymethyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)acetate

Guidance literature:: Multi-step reaction with 6 steps

1: isopropyl alcohol / 18 h / 20 °C / Inert atmosphere

2: acetic acid; nitric acid / water / 18 h / 20 °C / Inert atmosphere

3: ethanol / 150 °C / Microwave irradiation; Inert atmosphere

4: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h / 20 °C / Inert atmosphere

5: triethylamine / tetrahydrofuran / Inert atmosphere

6: sodium tetrahydroborate / water; tetrahydrofuran / Inert atmosphere

With sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; nitric acid; acetic acid; triethylamine; In tetrahydrofuran; ethanol; water; ethyl acetate; isopropyl alcohol;
DOI:10.1021/jm4008906

Reference yield:

: 915297-04-0
benzyl 6-(2-tert-butoxy-2-oxoethyl)-4-(2,4-dichlorophenyl)-2-methyl-5-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine-3-carboxylate

: 915297-06-2,915731-60-1,915731-61-2
tert-butyl 2-(4-(2,4-dichlorophenyl)-3-(hydroxymethyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 2 h / 20 °C / Inert atmosphere

2: triethylamine / tetrahydrofuran / Inert atmosphere

3: sodium tetrahydroborate / water; tetrahydrofuran / Inert atmosphere

With sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1021/jm4008906